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Coors Biomedical Co.

Country not established

Devices
7

What Coors Biomedical Co. makes

Coors Biomedical Co. manufactures bone graft substitutes and dental materials, including hydroxyapatite-based products for alveolar ridge augmentation. Their portfolio includes mesh and powder forms of hydroxyapatite for dental bone regeneration, such as OSTEOGRAF/AR and its variants, as well as dental porcelain powder for clinical applications.

These devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records. The company operates within the United States, where its products are listed in the FDA’s 510(k) registry.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue7

Newest first, rows 1-7 of 7

Frequently asked questions

How many devices does Coors Biomedical Co. have in the registry?

The registry currently lists 7 devices for Coors Biomedical Co.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Coors Biomedical Co.'s devices?

Among its 7 most recently registered devices, Coors Biomedical Co. has devices listed in FDA 510(k) (7 devices).

What risk classes do Coors Biomedical Co.'s devices fall under?

Among its 7 most recently registered devices, the classes recorded for Coors Biomedical Co.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Coors Biomedical Co. in the registry?

The most recently registered devices listed for Coors Biomedical Co. include OSTEOGRAF/AR AND OSTEOGRAF/AR+, OSTEOGRAF/AR+(PLUS) ALVEOLAR RID HYDROX 18-40 MESH, OSTEOGRAF AR ALVEOLAR RIDGE HYDROXYLAPATITE 18-40 and OSTEOGRAF/AR ALVEOLAR RID HYDROX, 18-40 MESH.

Generated automatically from registry data and not verified by a human reviewer.