Ceremed, Inc.
United StatesFDA applicant, unverified
- Devices
- 84
What Ceremed, Inc. makes
Ceremed, Inc. manufactures polyethylene-based craniofacial tissue reconstructive materials designed for reconstructive and aesthetic surgical applications in the head and facial region.
The company’s products are regulated under FDA Class II and Class III (U) devices, with submissions supported via 510(k) clearances and Unique Device Identifiers (UDIs). These materials are listed in the FDA’s regulatory databases.
Catalogue
Search and filter all 84 devicesShowing 1-50 of 84
Company details
- DUNS number
- 626959824
- info@ceremed.com
- Phone
- 310-815-2125
Frequently asked questions
How many devices does Ceremed, Inc. have in the registry?
The registry currently lists 84 devices for Ceremed, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ceremed, Inc.'s devices?
Among its 50 most recently registered devices, Ceremed, Inc. has devices listed in FDA GUDID (50 devices).
What risk classes do Ceremed, Inc.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for Ceremed, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ceremed, Inc. in the registry?
The most recently registered devices listed for Ceremed, Inc. include Biopor® UCR-9064, Biopor® CSL-4052, Biopor® USH-0554 and Biopor® CSP-0016.