Belega, Inc.
JapanFDA applicant, unverified
- Devices
- 5
What Belega, Inc. makes
Belega, Inc. manufactures transcutaneous neuromuscular electrical stimulation (TENS) systems designed for physical therapy applications, including the BEAGANK 4T PLUS and its attachments like the SCALP ATTACHMENT and SMALL ATTACHMENT. These devices deliver targeted electrical stimulation to promote muscle activation and rehabilitation.
The company’s products are regulated as Class II medical devices in the US, authorised through FDA pathways including 510(k) clearance and the Unique Device Identifier (UDI) system. The portfolio is listed under these regulatory mechanisms, and the manufacturer is based in the United States.
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
Beagank 4T Plus Ref K233010
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Belega, Inc. have in the registry?
The registry currently lists 5 devices for Belega, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Belega, Inc.'s devices?
Among its 5 most recently registered devices, Belega, Inc. has devices listed in FDA 510(k) (1 device) and FDA GUDID (4 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Belega, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Belega, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Belega, Inc. in the registry?
The most recently registered devices listed for Belega, Inc. include BEAGANK 4T PLUS 4TP-OTC, BEAGANK 4T PLUS 4TP-OTC-M, SCALP ATTACHMENT 4TP-OTC-C and SMALL ATTACHMENT 4TP-OTC-S.