Kinamed, Incorporated
United StatesFDA applicant, unverified
- Devices
- 2
What Kinamed, Incorporated makes
Kinamed, Incorporated manufactures the SuperCable® Iso-Elastic™ Cerclage System, a surgical device used for internal fixation of soft tissue or bone, including spinal and orthopedic applications. The ISO-ELASTIC CERCLAGE SYSTEM (1MM and 2MM cable diameter) is designed to provide tensioned stabilization in procedures requiring secure ligament or tendon repair.
The company’s devices fall under FDA Class II regulation and are listed via the 510(k) pathway. Kinamed, Incorporated is based in the United States.
Catalogue
SuperCable® Iso-Elastic™ Cerclage System Ref K181749
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Kinamed, Incorporated have in the registry?
The registry currently lists 2 devices for Kinamed, Incorporated. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kinamed, Incorporated's devices?
Among its 2 most recently registered devices, Kinamed, Incorporated has devices listed in FDA 510(k) (2 devices).
What risk classes do Kinamed, Incorporated's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Kinamed, Incorporated's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kinamed, Incorporated in the registry?
The most recently registered devices listed for Kinamed, Incorporated include SuperCable® Iso-Elastic™ Cerclage System and ISO-ELASTIC CERCLAGE SYSTEM (1MM AND 2MM CABLE DIAMETER).