Zeniva® ZA-500 L is a lubricated grade of polyetheretherketone (PEEK) offered for use in implantable devices. The manufacturing facility for Zeniva® PEEK in Alpharetta, GA is ISO 13485 registered and the relevant aspects of current Good Manufacturing Practices are also applied. Our biomaterial manufacturing processes are carefully validated, and enhanced controls provide product traceability. In addition, all materials are tested in a lab that is ISO 17025 accredited. This product meets the requirements of the current version of ASTM F 2026. Zeniva® ZA-500 L is offered as resin pellets and fabricated forms such as rods and plates. The chemical, physical, and mechanical properties of finished parts are related to the processes utilized in producing the finished part (for example, molding, machining, annealing, sterilization, etc). An FDA MAF is available.

Zeniva® ZA-500 is a grade of polyetheretherketone (PEEK) offered for use in implantable devices. The manufacturing facility for Zeniva® PEEK in Alpharetta, GA is ISO 13485 registered and the relevant aspects of current Good Manufacturing Practices are also applied. Our biomaterial manufacturing processes are carefully validated, and enhanced controls provide product traceability. In addition, all materials are tested in a lab that is ISO 17025 accredited. This product meets the requirements of the current version of ASTM F 2026. Zeniva® ZA-500 is offered as resin pellets and fabricated forms such as rods and plates. The chemical, physical, and mechanical properties of finished parts are related to the processes utilized in producing the finished part (for example, molding, machining, annealing, sterilization, etc). An FDA MAF is available and a PMDA MF is available in Japan.

Zeniva® ZA-500 is a grade of polyetheretherketone (PEEK) offered for use in implantable devices. The manufacturing facility for Zeniva® PEEK in Alpharetta, GA is ISO 13485 registered and the relevant aspects of current Good Manufacturing Practices are also applied. Our biomaterial manufacturing processes are carefully validated, and enhanced controls provide product traceability. In addition, all materials are tested in a lab that is ISO 17025 accredited. This product meets the requirements of the current version of ASTM F 2026. Zeniva® ZA-500 is offered as resin pellets and fabricated forms such as rods and plates. The chemical, physical, and mechanical properties of finished parts are related to the processes utilized in producing the finished part (for example, molding, machining, annealing, sterilization, etc). An FDA MAF is available and a PMDA MF is available in Japan.

Zeniva® ZA-520 is a grade of polyetheretherketone (PEEK) offered for use in implantable devices. This grade of Zeniva® PEEK is an Image Contrast grade, offering a level of opacity for imaging techniques such as MRI, CT and X-ray. The manufacturing facility for Zeniva® PEEK in Alpharetta, GA is ISO 13485 registered and the relevant aspects of current Good Manufacturing Practices are also applied. Our biomaterial manufacturing processes are carefully validated, and enhanced controls provide product traceability. In addition, all materials are tested in a lab that is ISO 17025 accredited. The chemical, physical and mechanical properties of finished parts are related to the processes utilized in producing the finished part, for example, molding, machining, annealing, sterilization, etc. Zeniva® ZA520 is available in resin pellets and rods.

Zeniva® ZA-520 is a grade of polyetheretherketone (PEEK) offered for use in implantable medical devices. This grade of Zeniva® PEEK is an Image Contrast grade, offering a level of opacity for imaging techniques such as MRI, CT and X-ray. The manufacturing factily for Zeniva® PEEK in Alpharetta, GA is ISO 13485 registered and the relaevant aspects of current Good Manufacturing Practices are also applied. Our biomaterial manufacturing processes are carefully validated, and enhanced controls provide product traceability. In addition, all materials are tested in an accredited lab that is ISO 17025 compliant. The chemical, physical and mechanical properties of finished parts are related to the processes utilized in producing the finished part, for example, molding, machining, annealing, sterilzation.

Zeniva ® ZA-550 L is a grade of polyetheretherketone (PEEK) offered for use in implantable devices. Zeniva ® ZA-550 L has been optimized for conversion into extruded filament for use in Fused Filament printers. The manufacturing facility for Zeniva ® PEEK in Alpharetta, GA is ISO 13485 registered and the relevant aspects of current Good Manufacturing Practices are also applied. Our biomaterial manufacturing processes are carefully validated, and enhanced controls provide product traceability. In addition, all materials are tested in a lab that is ISO 17025 accredited. Zeniva ® ZA-550 L is offered as resin pellets. The chemical, physical, and mechanical properties of finished parts are related to the processes utilized in producing the finished part (for example; printing, molding, machining, annealing, sterilization, etc). An FDA MAF is available.

Zeniva® ZA-600 BK L is a lubricated grade of polyetheretherketone (PEEK) offered for use in implantable devices. The manufacturing facility for Zeniva® PEEK in Alpharetta, GA is ISO 13485 registered and the relevant aspects of current Good Manufacturing Practices are also applied. Our biomaterial manufacturing processes are carefully validated, and enhanced controls provide product traceability. In addition, all materials are tested in a lab that is ISO 17025 accredited. The chemical, physical, and mechanical properties of finished parts are related to the processes utilized in producing the finished part (for example, molding, machining, annealing, sterilization, etc). Zeniva® ZA-600 BK L is offered as resin pellets. An FDA MAF is available.

Zeniva® ZA-600 BK is a grade of polyetheretherketone (PEEK) offered for use in implantable devices. The manufacturing facility for Zeniva® PEEK in Alpharetta, GA is ISO 13485 registered and the relevant aspects of current Good Manufacturing Practices are also applied. Our biomaterial manufacturing processes are carefully validated, and enhanced controls provide product traceability. In addition, all materials are tested in a lab that is ISO 17025 accredited. The chemical, physical, and mechanical properties of finished parts are related to the processes utilized in producing the finished part (for example, molding, machining, annealing, sterilization, etc). Zeniva® ZA-600 BK is offered as resin pellets. An FDA MAF is available.

Zeniva® ZA-600 CF10 is a carbon-fiber reinforced grade of polyetheretherketone (PEEK) offered for use in implantable devices. The manufacturing facility for Zeniva® PEEK is ISO 13485 registered and the relevant aspects of current Good Manufacturing Practices are also applied. Our biomaterial manufacturing processes are carefully validated, and enhanced controls provide product traceability. In addition, all materials are tested in a lab that is ISO 17025 accredited. The chemical, physical, and mechanical properties of finished parts are related to the processes utilized in producing the finished part (for example, molding, machining, annealing, sterilization, etc). Zeniva® ZA-600 CF10 is offered as compounded pellets. An FDA MAF is available.

Zeniva® ZA-600 CF30 is a carbon-fiber reinforced grade of polyetheretherketone (PEEK) offered for use in implantable devices. The manufacturing facility for Zeniva® PEEK is ISO 13485 registered and the relevant aspects of current Good Manufacturing Practices are also applied. Our biomaterial manufacturing processes are carefully validated, and enhanced controls provide product traceability. In addition, all materials are tested in a lab that is ISO 17025 accredited. The chemical, physical, and mechanical properties of finished parts are related to the processes utilized in producing the finished part (for example, molding, machining, annealing, sterilization, etc). Zeniva® ZA-600 CF30 is offered as compounded pellets. An FDA MAF is available. In Japan, a PMDA MF is available.

Zeniva® ZA-600 L is a lubricated grade of polyetheretherketone (PEEK) offered for use in implantable devices. The manufacturing facility for Zeniva® PEEK in Alpharetta, GA is ISO 13485 registered and the relevant aspects of current Good Manufacturing Practices are also applied. Our biomaterial manufacturing processes are carefully validated, and enhanced controls provide product traceability. In addition, all materials are tested in a lab that is ISO 17025 accredited. This product meets the requirements of the current version of ASTM F 2026. The chemical, physical, and mechanical properties of finished parts are related to the processes utilized in producing the finished part (for example, molding, machining, annealing, sterilization, etc). Zeniva® ZA-600 L is offered as resin pellets. An FDA MAF is available.

Zeniva® ZA-600 is a grade of polyetheretherketone (PEEK) offered for use in implantable devices. The manufacturing facility for Zeniva® PEEK in Alpharetta, GA is ISO 13485 registered and the relevant aspects of current Good Manufacturing Practices are also applied. Our biomaterial manufacturing processes are carefully validated, and enhanced controls provide product traceability. In addition, all materials are tested in a lab that is ISO 17025 accredited. This product meets the requirements of the current version of ASTM F 2026. The chemical, physical, and mechanical properties of finished parts are related to the processes utilized in producing the finished part (for example, molding, machining, annealing, sterilization, etc). Zeniva® ZA-600 is offered as resin pellets. An FDA MAF is available.