Demetra, Inc.
Country not established FDA establishment FEI 3040266825
- Devices
- 37
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
Search and filter all 37 devicesCompany details
- FDA FEI number
- 3040266825
- Address
- 6800 Poplar Ave Ste 120, Germantown, TN, 38138
Frequently asked questions
How many devices does DEMETRA, INC. have in the registry?
The registry currently lists 37 devices for DEMETRA, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list DEMETRA, INC.'s devices?
Among its 37 most recently registered devices, DEMETRA, INC. has devices listed in FDA GUDID (37 devices).
What risk classes do DEMETRA, INC.'s devices fall under?
Among its 37 most recently registered devices, the classes recorded for DEMETRA, INC.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from DEMETRA, INC. in the registry?
The most recently registered devices listed for DEMETRA, INC. include Tailored-H Cervical Standalone System BCS7-1416-6, Tailored-H Cervical Standalone System BCS7-1416-7, Tailored-H Cervical Standalone System BCS7-1416-8 and Tailored-H Cervical Standalone System BCS7-1416-9.