Ceramed Dental, LLC
United StatesFDA applicant, unverified
- Devices
- 2
What Ceramed Dental, LLC makes
Ceramed Dental, LLC manufactures bone graft substitutes, specifically the OSTEOGRAF/N-300 and OSTEOGRAF/N-700, designed for dental and maxillofacial applications. These products are intended for use in bone regeneration procedures, providing a scaffold for new bone growth in surgical sites.
The company’s portfolio is regulated under Class II medical devices in the US, with devices listed via the FDA’s 510(k) clearance process. The manufacturer is based in the United States.
Catalogue
Osteograf/N-300 Ref K981182
Regimes: 510(k) Registry: 510(k)Osteograf/N-700 Ref K981214
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ceramed Dental, LLC have in the registry?
The registry currently lists 2 devices for Ceramed Dental, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ceramed Dental, LLC's devices?
Among its 2 most recently registered devices, Ceramed Dental, LLC has devices listed in FDA 510(k) (2 devices).
What risk classes do Ceramed Dental, LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Ceramed Dental, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ceramed Dental, LLC in the registry?
The most recently registered devices listed for Ceramed Dental, LLC include OSTEOGRAF/N-300 and OSTEOGRAF/N-700.