Kinetikos Medical, Inc.
United StatesFDA applicant, unverified
- Devices
- 19
What Kinetikos Medical, Inc. makes
Kinetikos Medical, Inc. manufactures orthopedic implants and surgical instrumentation, including bone screw systems, wrist fusion systems, and subtalar implants. Their product portfolio also features cement restrictor implants, hand surgery sets, and modifications for total wrist systems.
The company is based in the United States, and its devices are categorized as Class I, Class II, and U. These products are listed within the FDA 510(k) regulatory registry.
Catalogue
Search and filter all 19 devicesFrequently asked questions
How many devices does Kinetikos Medical, Inc. have in the registry?
The registry currently lists 19 devices for Kinetikos Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kinetikos Medical, Inc.'s devices?
Among its 19 most recently registered devices, Kinetikos Medical, Inc. has devices listed in FDA 510(k) (19 devices).
What risk classes do Kinetikos Medical, Inc.'s devices fall under?
Among its 19 most recently registered devices, the classes recorded for Kinetikos Medical, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kinetikos Medical, Inc. in the registry?
The most recently registered devices listed for Kinetikos Medical, Inc. include KMI WRIST FUSION SYSTEM, KMI CEMENT RESTRICTOR IMPLANT, K4 BONE SCREW SYSTEM and KOMPRESSOR SCREW SYSTEM.