Care Rehab, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Care Rehab, Inc. makes
Care Rehab, Inc. manufactures transcutaneous electrical nerve stimulation (TENS) devices, including the CARE TENS and CLASSIC TENS, which deliver low-voltage electrical pulses for pain management. The company also produces neuromuscular stimulation (NMS) units, such as the CLASSIC NMS, and interferential current therapy (IFC) devices like the CARE IFC PLUS, designed for muscle stimulation and pain relief.
These devices are classified as Class II under FDA regulations and are authorised via the 510(k) pathway. The portfolio is listed in the FDA’s 510(k) clearance registry, and the company is based in the United States.
Catalogue
Care Tens Ref K984025
Regimes: 510(k) Registry: 510(k)Classic Nms Ref K021905
Regimes: 510(k) Registry: 510(k)Care Ifc Plus Ref K020516
Regimes: 510(k) Registry: 510(k)Classic Tens Ref K020437
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Care Rehab, Inc. have in the registry?
The registry currently lists 4 devices for Care Rehab, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Care Rehab, Inc.'s devices?
Among its 4 most recently registered devices, Care Rehab, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Care Rehab, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Care Rehab, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Care Rehab, Inc. in the registry?
The most recently registered devices listed for Care Rehab, Inc. include CARE TENS, CLASSIC NMS, CARE IFC PLUS and CLASSIC TENS.