Medynus, Inc.
United StatesFDA applicant, unverified FDA FEI 3015426608
- Devices
- 276
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Medynus, Inc. makes
Medynus, Inc. manufactures bone‑screw internal spinal fixation systems, non‑sterile, including the Impeace Cervical Plate System series.
Its devices are listed in the FDA 510(k) premarket notification database and the FDA GUDID device identification database. The listed devices are recorded as Class II.
Catalogue
Search and filter all 276 devicesShowing 1-50 of 276
Company details
- FDA FEI number
- 3015426608
- DUNS number
- 094374525
- Address
- 18 Technology Dr. Suite 109, Irvine, CA, 92618
Frequently asked questions
How many devices does Medynus, Inc. have in the registry?
The registry currently lists 276 devices for Medynus, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medynus, Inc.'s devices?
Among its 50 most recently registered devices, Medynus, Inc. has devices listed in FDA GUDID (50 devices).
What risk classes do Medynus, Inc.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for Medynus, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medynus, Inc. in the registry?
The most recently registered devices listed for Medynus, Inc. include Impeace Cervical Plate System TP.PL.0110, Impeace Cervical Plate System TP.PL.0118, Impeace Cervical Plate System TP.PL.0114 and Impeace Cervical Plate System TP.PL.0120.