Medipost, Inc.
United Statesfrom the FDA registration address FDA establishment FEI 3042773073
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
Company details
- FDA FEI number
- 3042773073
- Address
- 245 Main St, Cambridge, MA, 02142
Frequently asked questions
How many devices does MEDIPOST, INC. have in the registry?
The registry currently lists 1 device for MEDIPOST, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list MEDIPOST, INC.'s devices?
Among its 1 most recently registered device, MEDIPOST, INC. has devices listed in FDA GUDID (1 device).
What risk classes do MEDIPOST, INC.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for MEDIPOST, INC.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from MEDIPOST, INC. in the registry?
The most recently registered devices listed for MEDIPOST, INC. include CARTISTEM® Subchondral Bone Drill Bit - 4mm.