Cefar Medical AB
Country not established
- Devices
- 2
What Cefar Medical AB makes
Cefar Medical AB manufactures electrotherapy devices, including the CEFAR PRIMO and the CEFAR REHAB 2 series (with the REHAB 2 PRO variant). These products are designed for physical therapy applications, such as muscle stimulation and pain management, using electrical currents to aid rehabilitation and recovery.
The company’s portfolio is classified under FDA’s Class II regulatory category and includes devices authorised via the 510(k) clearance process. These products are listed in the FDA’s 510(k) database, reflecting their compliance with U.S. medical device regulations. The manufacturer is based in the United States.
Catalogue
Cefar Medical Ab Cefar Primo Ref K020803
Regimes: 510(k) Registry: 510(k)Cefar Rehab 2 And Rehab 2 Pro Ref K030403
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cefar Medical AB have in the registry?
The registry currently lists 2 devices for Cefar Medical AB. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cefar Medical AB's devices?
Among its 2 most recently registered devices, Cefar Medical AB has devices listed in FDA 510(k) (2 devices).
What risk classes do Cefar Medical AB's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Cefar Medical AB's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cefar Medical AB in the registry?
The most recently registered devices listed for Cefar Medical AB include CEFAR MEDICAL AB CEFAR PRIMO and CEFAR REHAB 2 AND REHAB 2 PRO.