Maven Labs, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Maven Labs, Inc. makes
Maven Labs, Inc. manufactures transcutaneous electrical nerve stimulation (TENS) devices, including the RELIEFBAND TENS Unit and the RELIEF BAND, designed for pain management through low-voltage electrical impulses.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. Maven Labs, Inc. is based in the United States.
Catalogue
Reliefband Tens Unit (Modification) Ref K961050
Regimes: 510(k) Registry: 510(k)Relief Band (T.E.N.S. Device) Ref K901704
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Maven Labs, Inc. have in the registry?
The registry currently lists 2 devices for Maven Labs, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Maven Labs, Inc.'s devices?
Among its 2 most recently registered devices, Maven Labs, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Maven Labs, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Maven Labs, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Maven Labs, Inc. in the registry?
The most recently registered devices listed for Maven Labs, Inc. include RELIEFBAND TENS UNIT (MODIFICATION) and RELIEF BAND (T.E.N.S. DEVICE).