Liviwell, Inc.
United Statesfrom the FDA registration address FDA FEI 3044091160
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Livi Device Ref K252005
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3044091160
- Address
- 333 Us Highway 46 Ste 201, Mountain Lakes, NJ, 07046
Frequently asked questions
How many devices does Liviwell, Inc. have in the registry?
The registry currently lists 1 device for Liviwell, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Liviwell, Inc.'s devices?
Among its 1 most recently registered device, Liviwell, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Liviwell, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Liviwell, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Liviwell, Inc. in the registry?
The most recently registered devices listed for Liviwell, Inc. include Livi Device.