Meduloc
United Statesfrom the FDA registration address FDA establishment FEI 3042903229
- Devices
- 51
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
Search and filter all 51 devicesShowing 1-50 of 51
Company details
- FDA FEI number
- 3042903229
- Address
- 2010 Jimmy Durante Blvd Ste 200, Del Mar, CA, 92014
Frequently asked questions
How many devices does MEDULOC have in the registry?
The registry currently lists 51 devices for MEDULOC. Devices recorded under merged duplicate company entries are counted once.
Which registries list MEDULOC's devices?
Among its 50 most recently registered devices, MEDULOC has devices listed in FDA GUDID (50 devices).
What risk classes do MEDULOC's devices fall under?
Among its 50 most recently registered devices, the classes recorded for MEDULOC's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from MEDULOC in the registry?
The most recently registered devices listed for MEDULOC include Meduloc Intramedullary Fracture Fixation (IFF) System PKG-90-IFF-200015, Meduloc Intramedullary Fracture Fixation (IFF) System PKG-90-IFF-200515, Meduloc Intramedullary Fracture Fixation (IFF) System PKG-90-IFF-200020 and Meduloc Intramedullary Fracture Fixation (IFF) System PKG-90-IFF-200520.