# Coors Biomedical Co.

- Location (FDA's records): Lakewood, CO
- FDA decisions: 7 (1981–1986): 7 510(k) clearances
- Product codes: LYC (6), EIH (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 8 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Dentsply International, Inc.: 4 (https://510kreport.com/company/dentsply-international)
- Dio Department Dsi, Inc.: 2 (https://510kreport.com/company/dio-department-dsi)
- Bioform, Inc.: 2 (https://510kreport.com/company/bioform)

## Its most-cited devices
- K852742: Osteograf AR Alveolar Ridge Hydroxylapatite 18-40 (1985), cited by 3
- K862061: Osteograf/AR+ Permaridge Hydroxylapatite, 18-40 (1986), cited by 2
- K861084: Osteograf/AR Alveolar Rid Hydrox, 18-40 Mesh (1986), cited by 1
- K861083: Osteograf/AR+(Plus) Alveolar Rid Hydrox 18-40 Mesh (1986), cited by 1
- K863176: Additional Clinical Usages for Osteograf/AR & AR+ (1986), cited by 1

## Recent decisions
- K863176: Additional Clinical Usages for Osteograf/AR & AR+ (Nov 26, 1986)
- K862324: Osteograf/AR and Osteograf/AR+ (Aug 15, 1986)
- K862061: Osteograf/AR+ Permaridge Hydroxylapatite, 18-40 (Jul 29, 1986)
- K861084: Osteograf/AR Alveolar Rid Hydrox, 18-40 Mesh (Apr 30, 1986)
- K861083: Osteograf/AR+(Plus) Alveolar Rid Hydrox 18-40 Mesh (Apr 30, 1986)
- K852742: Osteograf AR Alveolar Ridge Hydroxylapatite 18-40 (Sep 26, 1985)
- K810822: Dental Porcelain Powder (Apr 21, 1981)

Source page: https://510kreport.com/company/coors-biomedical