FDA applicant

Coors Biomedical Co.

Lakewood, CO7 decisions1981–19860 recalls

FDA records 7 decisions for Coors Biomedical Co. (Lakewood, CO) from 1981 to 1986: 7 510(k) clearances. Most are in product codes LYC (Bone Grafting Material, Synthetic) and EIH (Powder, Porcelain). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, dental panel, where it files most

How often FDA has decided Coors Biomedical Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Coors Biomedical Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Coors Biomedical Co. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Coors Biomedical Co.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?