Centermed, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Centermed, Inc. makes
Centermed, Inc. makes the CenterMed Patient Matched Assisted Surgical Planning (ASP) System, a device used for surgical planning based on patient-specific anatomy.
The CenterMed Patient Matched Assisted Surgical Planning (ASP) System is classified as a Class II medical device and is listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Centermed, Inc. have in the registry?
The registry currently lists 2 devices for Centermed, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Centermed, Inc.'s devices?
Among its 2 most recently registered devices, Centermed, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Centermed, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Centermed, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Centermed, Inc. in the registry?
The most recently registered devices listed for Centermed, Inc. include CenterMed Patient Matched Assisted Surgical Planning (ASP) System.