Truro'S Ent.
CanadaFDA 510(k) applicant, unverified
- Devices
- 1
What Truro'S Ent. makes
Truro’s Ent. manufactures the Bodyflex Massager, a Class I electrotherapy device designed for muscle relaxation and pain relief through targeted vibration and massage therapy.
The Bodyflex Massager is regulated under the FDA’s 510(k) pathway as a Class I device and is listed in the U.S. regulatory database. The company is based in the United States.
Catalogue
Bodyflex Massager Ref K952041
510(k) 510(k)
Frequently asked questions
How many devices does Truro'S Ent. have in the registry?
The registry currently lists 1 device for Truro'S Ent.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Truro'S Ent.'s devices?
Among its 1 most recently registered device, Truro'S Ent. has devices listed in FDA 510(k) (1 device).
What risk classes do Truro'S Ent.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Truro'S Ent.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Truro'S Ent. in the registry?
The most recently registered devices listed for Truro'S Ent. include BODYFLEX MASSAGER.