Ceramed Corp.
United StatesFDA applicant, unverified
- Devices
- 17
What Ceramed Corp. makes
Ceramed Corp. manufactures bone graft substitutes and surgical instruments, including hydroxylapatite matrices (e.g., PERMAMESH-D, PERMARIDGE) and natural/periodontal hydroxylapatite granules (e.g., OSTEOGRAFT/N, OSTEOGRAFT/P). Their portfolio also includes stainless steel syringes (e.g., OSTEOGRAF) designed for delivering bone graft materials during orthopedic or periodontal procedures.
The company’s devices are regulated under FDA Class II and Class III classifications, with authorisation via 510(k) clearances and PMA submissions. Products are listed in the FDA’s regulatory databases, and the manufacturer is based in the United States.
Catalogue
Search and filter all 17 devicesFrequently asked questions
How many devices does Ceramed Corp. have in the registry?
The registry currently lists 17 devices for Ceramed Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ceramed Corp.'s devices?
Among its 17 most recently registered devices, Ceramed Corp. has devices listed in FDA 510(k) (16 devices) and FDA PMA (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Ceramed Corp.'s devices fall under?
Among its 17 most recently registered devices, the classes recorded for Ceramed Corp.'s devices are Class II and Class III. Each device page shows its own class and authorisation.
What are the newest devices from Ceramed Corp. in the registry?
The most recently registered devices listed for Ceramed Corp. include PERMAMESH-D HYDROXYLAPATITE MATRIX, OSTEOGRAF STAINLESS STEEL SYRING, PERMARIDGE SYRINGE and OSTEOGRAF/LD-300 HYDROXYLAPATITE.