Liviliti Health Products Corp
Also registered as LiViliti Health Products Corporation
United Statesfrom the FDA registration address FDA establishment FEI 3016784019
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Paptizer 360 Ref K252471
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3016784019
- Address
- 1680 Fruitville Rd Unit 557, Sarasota, FL, 34236
Frequently asked questions
How many devices does LIVILITI HEALTH PRODUCTS CORP have in the registry?
The registry currently lists 1 device for LIVILITI HEALTH PRODUCTS CORP. Devices recorded under merged duplicate company entries are counted once.
Which registries list LIVILITI HEALTH PRODUCTS CORP's devices?
Among its 1 most recently registered device, LIVILITI HEALTH PRODUCTS CORP has devices listed in FDA 510(k) (1 device).
What risk classes do LIVILITI HEALTH PRODUCTS CORP's devices fall under?
Among its 1 most recently registered device, the classes recorded for LIVILITI HEALTH PRODUCTS CORP's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from LIVILITI HEALTH PRODUCTS CORP in the registry?
The most recently registered devices listed for LIVILITI HEALTH PRODUCTS CORP include Paptizer 360.