| HS Code | 788636 |
| Product Name | Proto3000 Formlabs IBT Flex Resin |
| Manufacturer | Formlabs |
| Distributor | Proto3000 |
| Resin Type | Flexible biocompatible photopolymer resin |
| Intended Use | Indirect bonding trays for orthodontic bracket placement |
| Biocompatibility | Biocompatible for intraoral use |
| Color | Clear |
| Curing Wavelength | 405 nm |
| Printer Compatibility | Formlabs Form 3B, Form 3B+, and Form 4B |
| Layer Thickness | 100 microns |
| Post Cure Temperature | 60 °C |
| Post Cure Time | 30 minutes |
| Hardness | 80 Shore A |
| Ultimate Tensile Strength | 8.5 MPa |
| Elongation At Break | 120% |
| Flexural Modulus | 250 MPa |
| Tear Strength | 25 kN/m |
| Density | 1.05 g/cm³ |
| Viscosity | 1.5 Pa·s |
| Packaging Volume | 1 L |
| Storage Temperature | 18-28 °C |
| Shelf Life | 1 year |
As an accredited Proto3000 Formlabs IBT Flex Resin factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Proto3000 Formlabs IBT Flex Resin is supplied as one sealed 1 L cartridge in a labeled cardboard box. |
| Container Loading (20′ FCL) | 20′ FCL container loaded with palletized Proto3000 Formlabs IBT Flex Resin, securely strapped and light-protected for compliant chemical transport. |
| Shipping | Proto3000 Formlabs IBT Flex Resin is not classified as dangerous goods for transport. It ships in sealed, light-protected cartridges/bottles, packed upright with absorbent material. Ground or expedited service is available; avoid heat, sunlight, and freezing. Always verify current SDS and carrier requirements before shipping. |
| Storage | Store Proto3000 Formlabs IBT Flex Resin in its original, tightly closed container, upright, in a cool, dry, well-ventilated area away from direct sunlight and UV light. Maintain 18–28°C (64–82°F); do not freeze. Keep away from heat, sparks, flames, oxidizers, and incompatible materials. Protect from moisture and contamination. Observe shelf-life and local regulations. |
| Shelf Life | Shelf life is 12 months when stored in the original container under recommended cool, dry, well-ventilated conditions away from sunlight. |
Direct bracket transfer without a dimensional reference can shift the bracket slot by more than 100 µm when the tray base exceeds 2.5 mm; the conversion from intraoral scan to print-ready STL therefore retains a 50 µm tessellation tolerance and a fixed offset of 0.2 mm from the bracket pad to the inner tray surface. In labial metal twin bracket workflows, Proto3000 Formlabs IBT Flex Resin is printed on a Formlabs 3B/3B+ low-force stereolithography system at a layer thickness of 100 µm from the 100% as-supplied single-component cartridge; no reactive diluent, filler, or photoinitiator addition is specified because any monomer dilution would alter the crosslink density that controls tear propagation during tray removal. The printed tray is washed in 99% isopropyl alcohol for 20 minutes in a Form Wash, air-dried with oil-free compressed air, and post-cured in a Form Cure at 60°C for 60 minutes. Support removal follows a palatal-first sequence to avoid flexural stress at the bracket slots. Compliance for the finished device is documented under ISO 10993-5:2009 cytotoxicity and ISO 10993-10:2010 skin sensitization, with manufacturing controls under ISO 13485:2016. Terminal product types include full-arch labial indirect bonding trays for metal twin brackets, pre-welded molar tube transfer trays, and rebonding trays with occlusal stops.
Lingual bracket slots are offset toward the tongue, and the tray must wrap the incisal edge with a thin flexible hinge that does not spring back during bracket transfer. For this configuration, the resin is used at 100% as-supplied; the only process variable is not an additive but a post-cure time extension to 70 minutes at 60°C when the printed wall thickness exceeds 2.0 mm, and that extension is validated by the laboratory against the lot-specific batch certificate rather than by introducing monomer. The production process begins with a digital model that includes the lingual bracket bases and a 0.15 mm pressure-relief channel at the slot; the build platform is oriented with the tray base 10–30 degrees from horizontal to reduce suction forces and avoid peel-plane failure at the incisal edge. After printing and washing, uncured resin is removed from undercuts with a soft brush before post-cure; residual solvent is dried with oil-free compressed air at 2 bar. Compliance follows ISO 10993-23:2021 irritation testing for the final tray and the material supplier’s quality files under ISO 13485:2016. Terminal products are lingual bracket indirect bonding trays used with 22-mil slot lingual brackets, indirect bonding trays for customized lingual archwire stops, and single-bracket repositioning jigs.
| Compliance area | Standard designation | Application boundary for IBT Flex Resin trays |
|---|---|---|
| Cytotoxicity | ISO 10993-5:2009 | Finished single-use indirect bonding tray |
| Skin sensitization | ISO 10993-10:2010 | Full-arch and single-bracket transfer trays |
| Irritation | ISO 10993-23:2021 | Lingual trays and extended mucosal contact |
| Quality management | ISO 13485:2016 | Dental laboratory batch production and lot traceability |
| Reprocessing boundary | ISO 17664-1:2021 | Single-use classification; no sterilization cycle applied |
Ceramic bracket wings fracture when the tray is peeled too quickly because the resin’s Shore hardness after post-cure governs the force transfer to the bracket tie-wing. Therefore the tray base is reduced to 1.2 mm over the bracket wings and thickened to 1.8 mm in the lingual extension. The resin is loaded at 100%; no low-viscosity diluent is used, and the addition of 2% ethanol to lower viscosity is explicitly non-validated because it reduces green tear strength and creates micro-voids at the tray-bracket interface. Production process includes designing composite flash reservoirs with a 0.3 mm offset around each ceramic bracket pad; the printed tray is washed and post-cured at 60°C for 60 minutes, then inspected under 10× magnification for delamination at thin sections. Compliance includes ISO 10993-5:2009 and ISO 10993-10:2010 for the single-use tray, and when shipped to the clinic, ISO 13485:2016 lot traceability. Terminal product types are full-arch ceramic bracket transfer trays with pre-defined flash reservoirs, anterior aesthetic bracket placement guides, and mixed ceramic-metal transfer trays.
When accessory attachments are prescribed with clear aligners, the flexible template must release from cured composite without lifting the attachment from the enamel. IBT Flex Resin is used at 100% as supplied; no filler is compounded into the resin because the cured template must remain sufficiently translucent for light-curing through the template, and any particulate addition would scatter the 450–470 nm dental curing light. The production process begins with attachment geometry imported from aligner planning software; a 0.05 mm compensation is applied at the attachment undercut, and the template is printed at 100 µm layer thickness on a Formlabs 3B/3B+ system. After washing and post-curing at 60°C for 60 minutes, the template is trimmed to an equigingival margin and seated on the arch to verify passive fit. Compliance includes ISO 10993-5:2009 cytotoxicity and, where labial contact is prolonged, ISO 10993-23:2021 irritation. Terminal product types are clear aligner attachment positioning templates, composite button transfer trays, and precision guides for secondary aligner hooks. Published production data for this specific configuration is limited compared with labial bracket trays; orthodontic laboratories should qualify each attachment morphology against the manufacturer’s exposure settings before batch production.
Autoclave steam is contraindicated because the post-cured photopolymer network softens above 70°C and the tray geometry distorts across the arch length; this boundary is relevant when a clinic workflow calls for pre-operative disinfection rather than terminal sterilization. The resin is processed at 100% as supplied; no antimicrobial additive is incorporated, and the addition of chlorhexidine or hydrogen peroxide to the wash bath is not validated because residual oxidizing agents can accelerate surface degradation. The production process includes an additional terminal disinfection step: after post-curing at 60°C for 60 minutes, the tray is immersed in 70% ethanol for no more than 5 minutes and dried under laminar flow for 10 minutes. This process is limited to single-use trays and does not substitute for sterilization under ISO 17664-1:2021. Compliance includes ISO 10993-5:2009 and ISO 10993-10:2010, and the dental practice must document the single-use classification under EU MDR 2017/745 Annex VIII. Terminal product types are disinfected single-use indirect bonding trays for infection-control-sensitive orthodontic cases and single-bracket emergency rebonding trays.
A dental laboratory batch production of indirect bonding trays from Proto3000 Formlabs IBT Flex Resin differs from chairside printing in that build platform utilization and lot-level traceability determine the acceptance criteria. The resin is printed at 100% single-component photopolymer with no batch-to-batch mixing; each cartridge change is recorded against the order number and the printer serial number to maintain traceability under ISO 13485:2016. The production process uses Formlabs 3B/3B+ systems with build platforms nested for 8–12 full-arch trays per cycle; the wash sequence is extended to 25 minutes when multiple trays are loaded in a Form Wash because the solvent becomes resin-saturated faster in high-density batch processing. After post-curing, each tray is measured at three arch-width landmarks with a digital caliper; any deviation greater than 0.5 mm from the STL reference is rejected. Compliance for the final tray includes ISO 10993-5:2009, ISO 10993-10:2010, and ISO 10993-23:2021, with incoming material documentation maintained under ISO 13485:2016. Terminal product types are laboratory-fabricated indirect bonding trays shipped to orthodontic clinics under lot-specific packaging, mixed tray-and-model cases, and replacement trays for rebonding after bracket failure.
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Proto3000 supplies the Proto3000 Formlabs IBT Flex Resin as a low-durometer photopolymer for Formlabs low-force stereolithography systems. The product is used when a cured part must survive repeated flexural loading, compression, or snap-fit assembly without the localized tearing that occurs in rigid resins. The model designation is IBT Flex Resin; the material is sold in Formlabs-compatible cartridges and requires a resin-specific PreForm profile before printing. The formulation is distinct from Formlabs Flexible 80A and Formlabs Elastic 50A in its published durometer location and in the ratio of tensile strength to elongation. Because this is a third-party product, lot-specific data from the Proto3000 certificate of analysis is the controlling source for numerical specifications.
At incoming inspection, the cartridge should be conditioned in the printer bay until the resin reaches the temperature stated on the cartridge label. A cartridge placed directly from cold storage into a warm printer can generate higher meniscus viscosity at the build surface, which changes recoating thickness and can produce a visible horizontal boundary in the first layers. The cartridge should be inspected for settled solids or phase separation; if a clear supernatant layer is visible, the supplier’s documented rolling procedure should be used. Open cartridges should not be used beyond the supplier’s stated exposure interval, and unfiltered resin from a failed build should not be returned to the cartridge because partially polymerized particulate will create point defects in subsequent layers.
Durometer comparisons in flexible photopolymers are meaningful only when the test specimen is post-cured under the same UV dose and thermal history as the production part. Under ASTM D2240, Formlabs Flexible 80A is published at 80A and Formlabs Elastic 50A at 50A. The IBT Flex Resin is positioned by Proto3000 in a different elastomeric region; the exact Shore value is not to be inferred from the product name and must be taken from the current certificate of analysis. For design purposes, Shore hardness alone is insufficient because two materials with similar durometer can exhibit different tensile strength and tear behavior under ASTM D638-14 and ASTM D624. The table below shows the comparative published values for Formlabs resins; the IBT Flex column is intentionally lot-specific because no verified third-party numerical datasheet was available for citation at the time of writing.
| Property | Test Method | Formlabs Flexible 80A | Formlabs Elastic 50A | Proto3000 IBT Flex Resin |
|---|---|---|---|---|
| Shore hardness | ASTM D2240 | 80A | 50A | Lot-specific certificate of analysis |
| Tensile strength at break | ASTM D638-14 | 8.9 MPa | 3.2 MPa | Lot-specific certificate of analysis |
| Elongation at break | ASTM D638-14 | 120% | 160% | Lot-specific certificate of analysis |
| Tear strength | ASTM D624 | 24 kN/m | 11 kN/m | Lot-specific certificate of analysis |
Published data for this specific IBT Flex configuration is limited; engineers should not transfer Formlabs published tensile or tear values into IBT Flex validation documents. The supplier’s certificate of analysis remains the only acceptable source for batch acceptance. Where a production process is governed by ISO 9001 or ISO 13485, the certificate should be stored with the batch record and linked to the printer log, the post-cure cycle, and the inspection method. First-article validation on the actual printer is required because lot-to-lot changes in photoinitiator concentration can shift the working curve without changing the liquid resin appearance.
A durometer reading taken on a part thinner than 6.0 mm can reflect the hardness of the underlying support table rather than the resin. ASTM D2240 requires a specimen thickness sufficient to prevent substrate interference; for soft elastomers, the supplier’s certificate may specify a multi-layer specimen. The Shore A scale is also nonlinear at the low and high ends, so a difference of 5A at 80A is not equivalent to the same interval at 50A. Designers who select a flexible resin for dynamic fatigue should compare the full stress-strain response under ASTM D638-14 and the tear strength under ASTM D624 before durometer alone.
Formlabs Flexible 80A is generally selected for stiffer elastomeric parts such as tubing clips and snap-fit closures where tear strength and abrasion resistance are more important than low-force conformability. Formlabs Elastic 50A is selected for soft cushioning and seals that must fill a large gap or tolerate surface irregularities. The IBT Flex Resin is positioned for applications that require an intermediate balance; the actual dissimilarity with Formlabs materials is demonstrated by the lot-specific data. A production line that currently uses Flexible 80A should not assume that IBT Flex can be substituted without changing the offset allowance in a mating assembly.
Washing low-durometer photopolymers requires a solvent exposure limit different from rigid resins. Isopropyl alcohol at 99% or higher concentration is commonly used, but an over-long wash can swell the crosslinked network and leave a tacky surface that cannot be fully recovered by post-cure. The solvent interval shown in the IBT Flex technical data sheet is a maximum, not a target. After washing, residual solvent retained in blind holes, undercuts, or compression ribs plasticizes the cured surface; the local Shore A value can drop below the bulk reading. Post-wash drying should be confirmed by mass loss or by visual absence of solvent sheen on a matte surface before UV post-cure begins.
Compression set is the more sensitive indicator of under-cure for this class of material. A part that reaches the expected Shore A value may still exhibit unacceptable compression set under ASTM D395 Method B when the post-cure dose is non-uniform or when the UV chamber’s lamp output has degraded. Post-curing in a Form Cure or equivalent 405 nm chamber should be validated for the largest production part geometry, not only for a flat coupon. The edges of a thick rubber-like block receive different photon flux than the center; this gradient produces a softer core that can relax under sustained load. Radiometric verification at 405 nm should be recorded before each batch, and the post-cure time and temperature should be treated as dimensional controls.
Under-cured IBT Flex parts retain unreacted methacrylate groups, which can continue to crosslink during storage and cause late shrinkage. Over-curing, by contrast, reduces elongation at break and increases the probability of notched tear propagation from support marks or surface scratches. Therefore the post-cure cycle is not a generic step; it must match the supplier’s stated process and the final part thickness. Parts above 5 mm may require reduced layer thickness or extended gentle cure rather than a single high-intensity exposure, depending on the certificate of analysis.
For a Form Cure chamber, the nominal emission at 405 nm and the heated platform should be checked against an independent radiometer before each batch; lamp aging and reflectors can generate greater than 15% irradiance drift across the cavity. Large parts should be rotated if the chamber has no rotating platform. Under a non-uniform cure, one face of a gasket may develop a harder surface while the opposite face remains tacky; this condition is frequently misidentified as under-washing when it is actually under-cure. Process engineers should record post-cure temperature, duration, and peak irradiance in the batch record. If the part shows compressive set greater than the value specified in the certificate after a standard cycle, the post-cure cycle should not be extended without first checking the UV lamp output and the part’s residual solvent content.
Compression set is measured by deflecting a cylindrical specimen to a fixed strain under ASTM D395 Method B, generally at 23 °C or 70 °C for the specified aging period. A part with high compression set may continue to seal after short-term service but loses contact force after thermal cycling. For IBT Flex, the acceptance threshold is lot-specific. When the application requires 24 h continuous compression at 70 °C, the material should be tested in the final production geometry rather than on a standard plaque because internal voids and layer boundaries influence recovery. Published data for this specific configuration is limited; internal validation is required.
Support contact on low-durometer surfaces differs from rigid photopolymer support removal. The tear strength of the material is the limiting parameter for support tip size and spacing. Coarse support tips can initiate catastrophic tears during manual removal because the cured support is often stiffer than the surrounding low-crosslink network. The part should be oriented so that flexural surfaces are not parallel to the build platform in high-support-density regions. If a tear starts at a support tip, the part should be discarded or evaluated under ASTM D624 because the notch sensitivity of elastomeric photopolymers is high. Published data for this specific configuration is limited, so first-article tests should include notched tear specimens produced on the same build platform as the production geometry.
Finishing of IBT Flex parts proceeds with sharp side cutters or a scalpel, but the cut line should be located away from functional flexural hinges. Sanding or grit blasting is generally not recommended for low-durometer parts because abrasive media can open surface pores and create tear initiation sites. If surface smoothing is required, a brief solvent wipe may be used only if the solvent is listed in the supplier’s post-processing guide. All finishing should be performed before post-cure whenever possible; post-curing after sanding can seal the surface but will not repair microtears created during finishing.
Adhesion of elastomeric builds to the build platform is often higher than the tear strength of the green part. The part should be removed with a plastic scraper or the printer’s recommended tool. Aggressive metal blade removal can create subsurface tears that remain invisible until cyclic loading. The build platform should be inspected for residual cured islands after every printing campaign; a small island in the platform surface produces a stress concentration that can reroute the first layer and change the thickness of each subsequent layer. Calibrating the platform with the manufacturer’s routine is not optional after a flexible resin build.
Before post-cure, the printed part is in a green state with a lower tensile strength and higher elongation than the final cured network. Handling a green flexible part can permanently stretch or distort thin fins and sealing lips. If the part is allowed to rest under its own weight before post-cure, the unsupported overhangs may creep. The time between printing and post-cure should be controlled as a process variable. A lot that is printed at the end of a shift and left overnight in the build chamber may not have the same dimensions as a part that is washed and cured within the supplier’s stated interval.
Cartridge rheology is a production risk for unattended builds. The IBT Flex Resin certificate lists viscosity at 25 °C; significant upward drift from the certified value is often caused by low room temperature, moisture ingress, or partial polymerization after overwarm storage. In a low-force stereolithography system, increased viscosity changes recoating speed and can leave thin streaks or uncoated zones. If the printer firmware does not contain a calibrated viscosity compensation curve for third-party resins, the operator must control the room temperature and cartridge conditioning time rather than relying on automatic settings. A deviation greater than the tolerance stated by Proto3000 should trigger a pre-production check of the cartridge, tray, and build chamber temperature.
On a large-format Form 3L build, temperature gradients across the resin tray are more pronounced than on smaller platforms; a tray positioned near a draft or cooling vent can show variable part gloss and layer banding. Batch logs from production-scale stereolithography commonly record room temperature at start, mid-print, and end, along with the cartridge lot and the elapsed time since opening. When a new lot of IBT Flex Resin is introduced, the part dimensions and durometer should be re-established on a small validation coupon before the full build volume is committed. This is a boundary condition of third-party resin use in closed-loop Formlabs hardware.
On a production line running a Form 3L with multiple cartridges, lot-to-lot variation in flexible resin can appear as a shift in the support removal force rather than a visible change in printed appearance. That force is an indirect measure of crosslink density and solvent retention. A sudden increase in support removal force can indicate that the resin is over-curing in the green state; a sudden decrease can indicate under-cure or solvent swelling. Process engineers should log this qualitative force because it is often the first indication of a cartridge that has drifted outside the supplier’s acceptance range.
If the printed part is intended for medical device prototyping or production, the IBT Flex Resin must be supported by the supplier’s documentation for biocompatibility, not by assumption. The absence of a specific ISO 10993 test result in the certificate means the material has not been validated for patient-contact use. In an ISO 13485 environment, the resin lot, printer serial number, PreForm profile revision, wash solvent batch, and post-cure cycle are all part of the device history record. The product can be used for tooling and fixtures within a regulated facility without patient-contact validation, but the tooling must not shed particles into the final device. Cleaning validation of soft elastomeric fixtures is more complex than for metal fixtures because the resin surface can retain process fluids in micropores.
For industrial production not governed by medical standards, the principal compliance anchors are the resin’s safety data sheet and the applicable workplace exposure limits for cleaning solvents. The cartridges should be disposed of according to local cured and uncured photopolymer waste rules. The safety data sheet gives the flash point and viscosity, but the operator should also verify that the wash solvent drying area is ventilated below the occupational exposure limit. These compliance points are often missing from a basic product introduction and should be included in a production risk assessment.
Typical production uses for IBT Flex Resin include soft-touch tooling inserts, sealing gaskets that must recover after repeated compression, vibration-isolation mounts, and protective covers with snap-fit closures. In sealing applications, the compression set boundary under ASTM D395 and the tear strength under ASTM D624 control the service life more directly than Shore hardness. In snap-fit covers, the flexural hinge design should avoid sharp internal corners; stress concentrations at these corners reduce the number of cycles before tear propagation. The selection of a flexible photopolymer should be based on the complete post-cured stress-strain curve, not on the liquid resin appearance or the marketing durometer range.