Beshape Technologies, Ltd.
IsraelFDA applicant, unverified
- Devices
- 1
What Beshape Technologies, Ltd. makes
Beshape Technologies, Ltd. manufactures the BeShape One™ Device, a medical device designed for orthopedic applications, including spinal and extremity corrections.
The BeShape One™ Device is classified as a Class II product under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
BeShape One™ Device Ref K231628
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Beshape Technologies, Ltd. have in the registry?
The registry currently lists 1 device for Beshape Technologies, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Beshape Technologies, Ltd.'s devices?
Among its 1 most recently registered device, Beshape Technologies, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Beshape Technologies, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Beshape Technologies, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Beshape Technologies, Ltd. in the registry?
The most recently registered devices listed for Beshape Technologies, Ltd. include BeShape One™ Device.