K900-LV is a low-viscosity high-flow Polyetheretherketone. The material has excellent wear resistance, chemical resistance, high rigidity and dimensional stability.

K900-MV is a medium-viscosity Polyetheretherketone. The material has excellent wear resistance, chemical resistance, high rigidity and dimensional stability.

Article code KTA2007/351

WR® 300 is a carbon-fiber reinforced compression molded PEEK™ often selected by pump manufacturers and users for pump bushings and case or impeller wear rings. Maximum service life is achieved in clean. lubricated and/or moist environments. WR 300 allows the pump user to increase pump effiency by running tighter wear ring clearances while decreasing potential pump damage when pumps are cavitated or experience radial bearing failures.

WR ® 525 is a thermoplastic composite consisting of carbon fiber in a PEEK matrix. Because of its unique thermal expansion properties, WR ® 525 is ideal for use as impeller wear rings, bushings and case wear rings. WR ® 525 allows the pump user to increase pump efficiency by running tighter wear ring clearances, while decreasing potential pump damage when pumps are cavitated or experience down-line bearing failures. WR ® 525 is API 610 approved for (stationary/stationary and rotating) wear applications.

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.