Theragun, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Theragun, Inc. makes
Theragun, Inc. manufactures portable recovery devices, including the TheraFace LED and TheraFace Microcurrent systems for facial skincare treatments, as well as the RecoveryAir PRO, a handheld air compression device for muscle recovery and circulation support.
These devices are classified as Class II under FDA regulations and are authorised through the 510(k) clearance process. The company is based in the United States.
Catalogue
TheraFace LED Ref K212155
Regimes: 510(k) Registry: 510(k)TheraFace Microcurrent Ref K212238
Regimes: 510(k) Registry: 510(k)RecoveryAir PRO Ref K211745
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Theragun, Inc. have in the registry?
The registry currently lists 3 devices for Theragun, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Theragun, Inc.'s devices?
Among its 3 most recently registered devices, Theragun, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Theragun, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Theragun, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Theragun, Inc. in the registry?
The most recently registered devices listed for Theragun, Inc. include TheraFace LED, TheraFace Microcurrent and RecoveryAir PRO.