Globalcare Intl., Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Globalcare Intl., Inc. makes
Globalcare Intl., Inc. makes transcutaneous electrical nerve stimulation (TENS) devices, including the Globalcare Micro 11 and Microcare models, as well as electrical muscle stimulation (EMS) devices such as the Globalcare EMS. The company also produces electrodes, including the Globalcare Electrode, and related devices like the Global Care Micro II.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Globalcare Micro 11 And Microcare (Tens) Ref K903394
Regimes: 510(k) Registry: 510(k)Globalcare Ems Ref K913444
Regimes: 510(k) Registry: 510(k)Globalcare Electrode Ref K913373
Regimes: 510(k) Registry: 510(k)Global Care Micro Ii Ref K910244
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Globalcare Intl., Inc. have in the registry?
The registry currently lists 4 devices for Globalcare Intl., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Globalcare Intl., Inc.'s devices?
Among its 4 most recently registered devices, Globalcare Intl., Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Globalcare Intl., Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Globalcare Intl., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Globalcare Intl., Inc. in the registry?
The most recently registered devices listed for Globalcare Intl., Inc. include GLOBALCARE MICRO 11 AND MICROCARE (TENS), GLOBALCARE EMS, GLOBALCARE ELECTRODE and GLOBAL CARE MICRO II.