VESTAKEEP® 4000 GF30 is a glass fiber-re­inforced (30%) polyether ether ketone for injection molding. The semi-crystalline polymer features superior mechanical, thermal, and chemical resistance. Parts made from VESTAKEEP® 4000 GF30 are of low flammability. Pigmentation may affect the values.

VESTAKEEP® 4000 FP is an unreinforced, highviscosity polyether ether ketone fine powder. It can be used as a basic resin or in blends with different additives for manufacturing compression molding parts. The semi-crystalline polymer features superior thermal and chemical resistance. VESTAKEEP® 4000 FP is of low flammability. Pigmentation may affect values.

VESTAKEEP® 4000 P is an unreinforced, high-viscosity polyether ether ketone powder. The product is suitable for the manufacture of compounds or it can be used as scatter-powder for the manufacture of composites. The semi-crystalline polymer features superior thermal and chemical resistance. VESTAKEEP® 4000 P is of low flammability. Pigmentation may affect the values.

VESTAKEEP® 4500 G is a high viscosity, fast cristallization polyether ether ketone for injection molding and extrusion The semi-crystalline polymer features superior, thermal and chemical resistance. Parts made from VESTAKEEP® 4500 G are of low flammability. Pigmentation may affect values.

VESTAKEEP® 5000 CF30 is a carbon fiber reinforced (30%) polyether ether ketone for injection molding. The semi-crystalline polymer features superior mechanical, thermal, and chemical resistance. Parts made from VESTAKEEP® 5000 CF30 are of low flammability. Pigmentation may affect values.

VESTAKEEP® 5000 FP is an unreinforced, high viscosity polyether ether ketone fine powder. It can be used as a basic resin or in blends with different additives for manufacturing compression molding parts. The semi-crystalline polymer features superior, thermal and chemical resistance. VESTAKEEP® 5000 FP is of low flammability. Pigmentation may affect the values.

VESTAKEEP® 5000 P is an unreinforced, high-viscosity polyether ether ketone powder. The semi-crystalline polymer features superior thermal and chemical resistance. VESTAKEEP® 5000 P is of low flammability. Pigmentation may affect the values.

VESTAKEEP® 50001XT BK is a high viscosity, unreinforced, unlubricated polyether ether ketone for injection molding and extrusion and can be cross-linked after processing by heat treatment. The semi-crystalline polymer features superior property retention at elevated temperatures combined with the chemical resistance of standard PEEK. Parts made from VESTAKEEP® 50001XT BK feature a very high resistance to creep.

VESTAKEEP® 5000 G is a high viscosity, unreinforced polyether ether ketone for injection molding and extrusion. The semi-crystalline polymer features superior, thermal and chemical resistance. Parts made from VESTAKEEP® 5000 G are of low flammability. Pigmentation may affect values.

VESTAKEEP® Care is the ideal materials for the fabrication of medical devices with short time contact to human blood, tissue or bone for up to 30 days. VESTAKEEP® Care Grades have a good biocompatibility, processability and the option to pigment. VESTAKEEP® Care M20 G black is a medium viscosity, unreinforced polyether ether ketone for injection molding. The semi-crystalline polymer features superior thermal and chemical resistance. Biocompatibility of VESTAKEEP® Care In an extensive testing program run by independent certified labs, biocompatibility has been tested following United States Pharmacopeia and ISO 10933-1:2003 guidelines. The test reports attest VESTAKEEP® Care's excellent biocompatibility.

VESTAKEEP® Care is the ideal materials for the fabrication of medical devices with short time contact to human blood, tissue or bone for up to 30 days. VESTAKEEP® Care Grades have a good biocompatibility, processability and the option to pigment. VESTAKEEP® Care M20 G is a medium viscosity, unreinforced polyether ether ketone for injection molding. The semi-crystalline polymer features superior thermal and chemical resistance. Biocompatibility of VESTAKEEP® Care In an extensive testing program run by independent certified labs, biocompatibility has been tested following United States Pharmacopeia and ISO 10933-1:2003. The test reports attest VESTAKEEP® Care's excellent biocompatibility.

VESTAKEEP® Care-grades are ideal materials for the fabrication of medical devices with short time contact to human blood, tissue or bone for up to 30 days. VESTAKEEP® Care M33G-HP is a mediumviscosity, unreinforced polyether ether ketone for injection molding and extrusion. The product is refined by Evonik’s special filtration technology. The semi-crystalline polymer features superior thermal and chemical resistance. Parts made from VESTAKEEP® Care M33G-HP are of low flammability. VESTAKEEP® Care M33 G-HP can be processed by common machines for thermoplastics. Biocompatibility of VESTAKEEP® Care In an extensive testing program run by independent certified labs, biocompatibility has been tested following United States Pharmacopeia an dISO 10933-1:2003 guidelines. The test reports attest VESTAKEEP® Care's excellent biocompatibility.

VESTAKEEP® Care M40 3DF is extruded from naturally colored, high viscosity VESTAKEEP® Care M40 G PEEK resin. The material is designed for 3d printing of medical devices with up to 30 days body contact. Biocompatibility The biocompatibility of the base resin VESTAKEEP® Care 40 G has been tested following ISO 10993-1 recommendations for medical devices with up to 30 days of body contact and USP Class VI. A summary of biocompatibility test results is available upon request.

VESTAKEEP® Care is the ideal materials for the fabrication of medical devices with short time contact to human blood, tissue or bone for up to 30 days. VESTAKEEP® Care Grades have a good biocompatibility, processability and the option to pigment. VESTAKEEP® Care M40 G is a high viscosity, unreinforced polyether ether ketone for injection molding and extrusion. The semi-crystalline polymer features superior thermal and chemical resistance. Biocompatibility of VESTAKEEP® Care In an extensive testing program run by independent certified labs, biocompatibility has been tested following United States Parmacopeia and ISO 10933-1:2003 guidelines. The test reports attest VESTAKEEP® Care's excellent biocompatibility.

VESTAKEEP® Care is the ideal materials for the fabrication of medical devices with short time contact to human blood, tissue or bone for up to 30 days. VESTAKEEP® Care Grades have a good biocompatibility, processability and the option to pigment. VESTAKEEP® Care M40 R are semi finished goods based on the high viscosity VESTAKEEP® Care M40 G polymer resin. The semi-crystalline polymer features superior thermal and chemical resistance. Biocompatibility of VESTAKEEP® Care In an extensive testing program run by independent certified labs, biocompatibility has been tested following United States Pharmacopeia and ISO 10933-1:2003 guidelines. The test reports attest VESTAKEEP® Care's excellent biocompatibility.

VESTAKEEP® D4 G is natural colored, high viscosity polyether ether ketone (PEEK) that is especially designed for removable and fixed dentures, crowns and bridges. Biocompatibility of VESTAKEEP® Dental For VESTAKEEP® D4 G, biocompatibility has been tested following ISO 10993-1 recommendations for permanent mucous membrane contact. The composition is optimised for high biocompatibility and superior mechanical, thermal and chemical resistance.

VESTAKEEP® D4 R is natural colored polyether ether ketone (PEEK) rod stock that is especially designed for removable and fixed dentures crowns and bridges. Biocompatibility of VESTAKEEP® Dental For VESTAKEEP® D4 R, biocompatibility has been tested following ISO 10993-1 recommendations for permanent mucous membrane contact. The composition is optimised for high biocompatibility and superior mechanical, thermal and chemical resistance.

VESTAKEEP® DC4420 G white pigmented polyether ether ketone for dental applications high viscosity polyether ether ketone (PEEK) resin that is especially designed for removable and fixed dentures, crowns and bridges. Biocompatibility of VESTAKEEP® Dental For VESTAKEEP® DC4420 G, biocompatibility has been tested according to ISO 10993-1 recommendations for permanent mucous membrane contact. The compound composition is optimised for high biocompatibility and superior mechanical, thermal and chemical resistance.

VESTAKEEP® DC4420 R is a white pigmented polyether ether ketone (PEEK) grade rod stock that is especially designed for removable and fixed dentures, crowns and bridges. Biocompatibility of VESTAKEEP® Dental For VESTAKEEP® DC4420 R, biocompatibility has been tested following ISO 10993-1 recommendations for permanent mucous membrane contact. The compound composition is optimised for high biocompatibility and superior mechanical, thermal and chemical resistance.

VESTAKEEP® DC4430 G is a white pigmented high viscosity polyether ether ketone (PEEK) resin that is especially designed for removable and fixed dentures, crowns and bridges. VESTAKEEP® DC4430 G contains 6% Barium sulphate to render it x-ray opaque. Biocompatibility of VESTAKEEP® Dental For VESTAKEEP® DC4430 G, biocompatibility has been tested according to ISO 10993-1 recommendations for permanent mucous membrane contact. The compound composition is optimised for high biocompatibility and superior mechanical, thermal and chemical resistance.

VESTAKEEP® DC4430 R is a white pigmented polyether ether ketone (PEEK) grade that is especially designed for removable and fixed dentures, crowns and bridges. VESTAKEEP® DC4430 R contains 6% Barium sulphate to render it x-ray opaque. Biocompatibility of VESTAKEEP® Dental For VESTAKEEP® DC4430 R, biocompatibility has been tested following ISO 10993-1 recommendations for permanent mucous membrane contact. The compound composition is optimised for high biocompatibility and superior mechanical, thermal and chemical resistance.

VESTAKEEP® DC4450 G is a tooth-colored, high viscosity polyether ether ketone (PEEK) resin that is especially designed for removable and fixed dentures, crowns and bridges. Biocompatibility of VESTAKEEP® Dental For VESTAKEEP® DC4450 G, biocompatibility has been tested according to ISO 10993-1 recommendations for permanent mucous membrane contact. The compound composition is optimised for high biocompatibility and superior mechanical, thermal and chemical resistance.

VESTAKEEP® DC4450 R is a tooth-colored polyether ether ketone (PEEK) grade that is especially designed for removable and fixed dentures, crowns and bridges. Biocompatibility of VESTAKEEP® Dental For VESTAKEEP® DC4450 R, biocompatibility has been tested following ISO 10993-1 recommendations for permanent mucous membrane contact. The compound composition is optimised for high biocompatibility and superior mechanical, thermal and chemical resistance.

VESTAKEEP® DC4460 G is a tooth-colored, high viscosity polyether ether ketone (PEEK) resin that is especially designed for removable and fixed dentures, crowns and bridges. VESTAKEEP® DC4460 G contains 6% Barium sulphate to render it x-ray opaque. Biocompatibility of VESTAKEEP® Dental For VESTAKEEP® DC4450 G, biocompatibility has been tested according to ISO 10993-1 recommendations for permanent mucous membrane contact. The compound composition is optimised for high biocompatibility and superior mechanical, thermal and chemical resistance.

VESTAKEEP® DC4460 R is a tooth-colored polyether ether ketone (PEEK) grade that is especially designed for removable and fixed dentures, crowns and bridges. VESTAKEEP® DC4460 R contains 6% Barium sulphate to render it x-ray opaque. Biocompatibility For VESTAKEEP® DC4460 R, biocompatibility has been tested following ISO 10993-1 recommendations for permanent mucous membrane contact. The compound composition is optimised for high biocompatibility and superior mechanical, thermal and chemical resistance.

VESTAKEEP® DC4462 G is a tooth-colored, high viscosity polyether ether ketone (PEEK) resin that is especially designed for removable and fixed dentures, crowns and bridges. VESTAKEEP® DC4462 G contains 15% barium sulphate to render it x-ray opaque. Biocompatibility For VESTAKEEP® DC4462 G, biocompatibility has been tested according to ISO 10993-1 recommendations for permanent mucous membrane contact. The compound composition is optimised for high biocompatibility and superior mechanical, thermal and chemical resistance.

VESTAKEEP® DC4470 G is a gingiva-colored, high viscosity polyether ether ketone (PEEK) resin that is especially designed for removable dentures to meet the aesthetic demands of the patient. Biocompatibility of VESTAKEEP® Dental For VESTAKEEP® DC4470 G, biocompatibility has been tested according to ISO 10993-1 recommendations for permanent mucous membrane contact. The compound composition is optimised for high biocompatibility and superior mechanical, thermal and chemical resistance.

VESTAKEEP® DC4470 R is a gingiva-colored polyether ether ketone (PEEK) grade that is especially designed for removable dentures to meet the aesthetic demands of the patient. Biocompatibility of VESTAKEEP® Dental For VESTAKEEP® DC4470 R, biocompatibility has been tested following ISO 10993-1 recommendations for permanent mucous membrane contact. The compound composition is optimised for high biocompatibility and superior mechanical, thermal and chemical resistance.

VESTAKEEP® Easy Slide I is a carbon fiber-reinforced, wear and friction modified polyether ether ketone for injection molding. The semi-crystalline polymer features superior, thermal and chemical resistance. Parts made from VESTAKEEP® Easy Slide I are flame resistant and can be used for bearing bushing or gearbox parts due to the self-lubricating effect. VESTAKEEP® Easy Slide I can be processed by common machines for thermoplastics.

VESTAKEEP® i2 G is a natural colored, standard viscosity polyether ether ketone (PEEK) that is especially designed for long term implantable medical devices. This grade is often used for injection molding processing technologies due to its good flowability. Proven Biocompatibility of VESTAKEEP® i-Grades The extra high purity and extended quality measures make VESTAKEEP® i-Grade materials an excellent choice for permanent implants. For VESTAKEEP® i2 G, biocompatibility has been tested following ISO 10993-1 recommendatins for permanent tissue/bone contact and USP Class VI. VESTAKEEP® i2 G complies ASTM F2026 "Standard Specification for Polyetheretherketon (PEEK) Polymers for Surgical Implant Application". A summary of biocompatibility test results is available upon request.

VESTAKEEP® i2 P is a medium-viscosity polyether ether ketone (PEEK) powder that is designed for long term human implant applications. Proven Biocompatibility of VESTAKEEP® i-Grades VESTAKEEP® i2 P is compliant with ASTM F2026 "Standard Specification for Polyetherketone (PEEK) Polymers for Surgical Implant Applications" The extra high purity and extended quality measures make the i-grades an ideal material for long term body contact. A summary of biocompatibility tests is available upon request.

VESTAKEEP® i2 UFP10 is an unreinforced, medium-viscosity, natural colored polyether ether ketone (PEEK) ultra-fine powder. VESTAKEEP® i2 UFP10 is especially designed for long term implantable medical devices. The semi-crystalline polymer is designed for high biocompatibility and superior mechanical, thermal and chemical resistance. Proven Biocompatibility of VESTAKEEP® i-Grades The biocompatibility of VESTAKEEP® i2 UFP10 has been tested following ISO `10993 recommendations for permanent tissue/bone contact. The material complies USP Class VI. VESTAKEEP® i2 UFP10 is compliant with ASTM F2026 "Standard Specification for Polyetherketone (PEEK) Polymers for Surgical Implant Applications". A summary of biocompatibility tests is available upon request.

VESTAKEEP® i4 3DF is a filament extruded from natural colored, high viscosity VESTAKEEP® i4 G polyether ether ketone (PEEK) resin. The material is especially designed for long term implantable medical devices. Proven Biocompatibility of VESTAKEEP® i-Grades The extra high purity and extended quality measures make VESTAKEEP® i-grade materials an excellent choice for permanent implants. The biocompatibility is the base resin VESTAKEEP® i4 G has been tested following ISO 10993-1 recommendations for permanent tissue/bone contact and USP Class VI. A summary of biocompatibility test results available upon request. VESTAKEEP® i4 3DF filaments are compliant to ASTM F2026 "Standard Specification for Polyether ether ketone (PEEK) Polymers for Surgical Implant Applications"

VESTAKEEP® i4 3DF-T is a filament extruded from natural colored, high viscosity VESTAKEEP® i4 G polyether ether ketone (PEEK) resin. The material is a testing grade designed for research, development and process optimization only. It must not be used for medical devices. The purpose of the testing grade is to offer a cost-efficient solution for printing process development. The testing grade VESTAKEEP® i4 3DF-T and the implantable grade VESTAKEEP® i4 3DF are both extruded from implantable-grade VESTAKEEP® i4 G resin. They share the same base resin, processability and mechanical properties.

VESTAKEEP® i4 G is a natural colored, high viscosity polyether ether ketone (PEEK) that is especially designed for long term implantable medical devices. This grade is often used for extrusion processing technologies. Proven Biocompatibility of VESTAKEEP® i-Grades The extra high purity and extended quality measures make VESTAKEEP® i-Grade materials an excellent choice for permanent implants. For VESTAKEEP® i4 G, biocompatibility has been tested following ISO 10993-1 recommendations for permanent tissue/bone contact and USP Class VI. VESTAKEEP® i4 G complies ASTM F2026 "Standard Specification for Polyetheretherketone (PEEK) Polymers for Surgical Implant Applications". A summary of biocompatibility test results is available upon request.

VESTAKEEP® i4P is a high-viscosity polyether ether ketone (PEEK) powder that is designed for long term human implant applications. Proven Biocompatibility of VESTAKEEP® i-Grades VESTAKEEP® i4 P is compliant with ASTM F2026 “Standard Specification for Polyetheretherketone (PEEK) Polymers for Surgical Implant Applications”. The extra high purity and extended quality measures make the i-grades an ideal material for long term body contact. A summary of biocompatibility tests is available upon request

VESTAKEEP® i4 PL are plates based on implantable grade VESTAKEEP® i4 G neat polyether ether ketone resin. Proven Biocompatibility of VESTAKEEP® i-Grades The extra high purity and extended quality measures make VESTAKEEP® i-Grade materials an excellent choice for permanent implants. For VESTAKEEP® i4 PL, biocomptibility has been tested according to ISO 10993-1 recommendations for permanent tissue/bone contact and USP Class VI. VESTAKEEP® i4 PL complies ASTM F2026 "Standard Specification for Polyethertherketone (PEEK) Polymers for Surgical Implant Applications" A summary of biocompatibility test results is available upon request.

VESTAKEEP® i4 R is a rod stock based on implantable grade neat polyether ether ketone resin VESTAKEEP® i4 G. Proven Biocompatibilty of VESTAKEEP® i-Grades The extra high purity and extended quality measures make VESTAKEEP® i-grade materials an excellent choice for permanent implants. The biocompatibility of VESTAKEEP® i4 R has been tested following ISO 10993-1 recommendations for permanent tissue/bone contact and USP Class VI. VESTAKEEP® i4 R complies to ASTM F2026 "Standard Specification for Polyetheretherketone (PEEK) Polymers for Surgical Implant Applications". A summary of biocompatibility test results is available upon request.

VESTAKEEP® i5 G is a natural colored, very high viscosity polyether ether ketone (PEEK) that is especially designed for long term implantable medical devices. The extra high purity and extended quality measures make VESTAKEEP® i-Grade materials an excellent choice for permanent implants. Proven Biocompatibility of VESTAKEEP® i-Grades The extra high purity and extended quality measures make VESTAKEEP® i-grade materials an excellent choice for permanent implants. The biocompatibility of VESTAKEEP® i5 G has been tested following ISO 10993-1 recommendations for permanent tissue/bone contact and USP Class VI. VESTAKEEP® i5 G complies to ASTM F2026 "Standard Specification for Polyetheretherketone (PEEK) Polymers for Surgical Implant Applications" A summary of biocompatibility test results is available upon request.

VESTAKEEP® i5 R is rod stock based on implantable grade neat polyether ether ketone resin VESTAKEEP® i5 G. The extra high purity and extended quality measures make VESTAKEEP® i-grade materials an excellent choice for permanent implants. Proven Biocompatibility of VESTAKEEP® i-Grades The extra high purity and extended quality measures make VESTAKEEP® i-grade materials an excellent choice for permanent implants. The biocompatibility of VESTAKEEP® i5 R has been tested following ISO 10993-1 recommendations for permanent tissue/bone contact and USP Class VI. VESTAKEEP® i5 R complies to ASTM F2026 "Standard Specification for Polyetheretherketone (PEEK) Polymers for Surgical Implant Applications" A summary of biocompatibility test results is available upon request.