Kinetic Biomedical Services, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
What Kinetic Biomedical Services, Inc. makes
Kinetic Biomedical Services, Inc. manufactures a range of medical devices, including the KINETIC MODEL 700, KINETIC MODEL 330, KINETIC MODEL 1000, KINETIC MODEL 500, and KINETIC MODEL 132. These devices appear to be designed for use in orthopedic or joint replacement procedures, likely as surgical instruments or implant systems.
The company’s portfolio is regulated under Class II devices in the US, with products listed via the FDA’s 510(k) pathway. These devices are recorded in the FDA’s 510(k) registry, and the manufacturer is based in the United States.
Catalogue
Kinetic Model 700 Ref K892808
Regimes: 510(k) Registry: 510(k)Kinetic Model 330 Ref K891759
Regimes: 510(k) Registry: 510(k)Kinetic Model 1000 Ref K891757
Regimes: 510(k) Registry: 510(k)Kinetic Model 500 Ref K891756
Regimes: 510(k) Registry: 510(k)Kinetic Model 132 Ref K891758
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Kinetic Biomedical Services, Inc. have in the registry?
The registry currently lists 5 devices for Kinetic Biomedical Services, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kinetic Biomedical Services, Inc.'s devices?
Among its 5 most recently registered devices, Kinetic Biomedical Services, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Kinetic Biomedical Services, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Kinetic Biomedical Services, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kinetic Biomedical Services, Inc. in the registry?
The most recently registered devices listed for Kinetic Biomedical Services, Inc. include KINETIC MODEL 700, KINETIC MODEL 330, KINETIC MODEL 1000 and KINETIC MODEL 500.