Thera Kinetics, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Thera Kinetics, Inc. makes
Thera Kinetics, Inc. manufactures continuous passive motion (CPM) devices for the knee and toe, including the JACE Model T300 (toe), JACE Model K200 (knee), and JACE Model 100 (knee). These devices are designed to assist in joint rehabilitation by promoting controlled, passive movement during recovery.
The company’s CPM devices are classified as Class I under FDA regulations and are supported by 510(k) clearance records. The portfolio is listed in the FDA’s 510(k) database, and the manufacturer is based in the United States.
Catalogue
Jace Model T300 Toe Cpm Device Ref K913227
Regimes: 510(k) Registry: 510(k)Jace Model K200 Knee Cpm Device, Modification Ref K912537
Regimes: 510(k) Registry: 510(k)Jace Model 100 Knee Cpm Device Ref K903467
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Thera Kinetics, Inc. have in the registry?
The registry currently lists 3 devices for Thera Kinetics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Thera Kinetics, Inc.'s devices?
Among its 3 most recently registered devices, Thera Kinetics, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Thera Kinetics, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Thera Kinetics, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Thera Kinetics, Inc. in the registry?
The most recently registered devices listed for Thera Kinetics, Inc. include JACE MODEL T300 TOE CPM DEVICE, JACE MODEL K200 KNEE CPM DEVICE, MODIFICATION and JACE MODEL 100 KNEE CPM DEVICE.