Bionicare Medical Technologies, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Bionicare Stimulator System, Model Bio-1000 Ref K052625
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Bionicare Medical Technologies, Inc. have in the registry?
The registry currently lists 2 devices for Bionicare Medical Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bionicare Medical Technologies, Inc.'s devices?
Among its 2 most recently registered devices, Bionicare Medical Technologies, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Bionicare Medical Technologies, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Bionicare Medical Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bionicare Medical Technologies, Inc. in the registry?
The most recently registered devices listed for Bionicare Medical Technologies, Inc. include BIONICARE STIMULATOR SYSTEM, MODEL BIO-1000 and MODIFICATION TO BIONICARE STIMULATOR SYSTEM, MODEL BIO-1000.