Endofix Medical Technologies
Country not established FDA establishment FEI 3031276312
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
- GUDID
- GUDID
Company details
- FDA FEI number
- 3031276312
- Address
- 111 Washington St. Suite 201i, Plainville, MA, 02762
Frequently asked questions
How many devices does ENDOFIX MEDICAL TECHNOLOGIES have in the registry?
The registry currently lists 2 devices for ENDOFIX MEDICAL TECHNOLOGIES. Devices recorded under merged duplicate company entries are counted once.
Which registries list ENDOFIX MEDICAL TECHNOLOGIES's devices?
Among its 2 most recently registered devices, ENDOFIX MEDICAL TECHNOLOGIES has devices listed in FDA GUDID (2 devices).
What risk classes do ENDOFIX MEDICAL TECHNOLOGIES's devices fall under?
Among its 2 most recently registered devices, the classes recorded for ENDOFIX MEDICAL TECHNOLOGIES's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from ENDOFIX MEDICAL TECHNOLOGIES in the registry?
The most recently registered devices listed for ENDOFIX MEDICAL TECHNOLOGIES include Secure Suture Locking Device D5000000 and EndoFix Tissue Fixation Device D6000000.