FDA applicant

Ceramed Corp.

Lakewood, CO17 decisions1989–19991 recall

FDA records 17 decisions for Ceramed Corp. (Lakewood, CO) from 1989 to 1999: 16 510(k) clearances and 1 original PMA approval. Most are in product codes LYC (Bone Grafting Material, Synthetic) and LZK (Implant, Malar). 1 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 Ceramed Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ceramed Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Ceramed”

FDA records each applicant name separately; these may or may not be the same firm.

Ceramed Dental, LLC 2

Ceramed Corp.

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?

What has been recalled?

Other applicant names beginning “Ceramed”