Life Prp
United Statesfrom the FDA registration address FDA establishment FEI 3033273466
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
Company details
- FDA FEI number
- 3033273466
- Address
- 2156 W Northwest Hwy Ste 305, Dallas, TX, 75220
Frequently asked questions
How many devices does LIFE PRP have in the registry?
The registry currently lists 3 devices for LIFE PRP. Devices recorded under merged duplicate company entries are counted once.
Which registries list LIFE PRP's devices?
Among its 3 most recently registered devices, LIFE PRP has devices listed in FDA GUDID (3 devices).
What risk classes do LIFE PRP's devices fall under?
Among its 3 most recently registered devices, the classes recorded for LIFE PRP's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from LIFE PRP in the registry?
The most recently registered devices listed for LIFE PRP include Life PRP LLC Centrifuge1, Life PRP LLC 24BC12ml and Life PRP LLC 1BC12ml.