Techmah Medical, LLC
United StatesFDA applicant, unverified
- Devices
- 3
What Techmah Medical, LLC makes
Techmah Medical, LLC manufactures the SmartSPACE Shoulder System, a device designed for shoulder rehabilitation and assessment, incorporating smart technology for monitoring and data collection during therapeutic exercises.
The SmartSPACE Shoulder System is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Smart SPACE Shoulder System Ref K202454
Regimes: 510(k) Registry: 510(k)Smart SPACE Shoulder System Ref K202151
Regimes: 510(k) Registry: 510(k)SmartSPACE Shoulder System Ref K191247
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Techmah Medical, LLC have in the registry?
The registry currently lists 3 devices for Techmah Medical, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Techmah Medical, LLC's devices?
Among its 3 most recently registered devices, Techmah Medical, LLC has devices listed in FDA 510(k) (3 devices).
What risk classes do Techmah Medical, LLC's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Techmah Medical, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Techmah Medical, LLC in the registry?
The most recently registered devices listed for Techmah Medical, LLC include Smart SPACE Shoulder System and SmartSPACE Shoulder System.