FDA applicant

Collagen Corp.

Palo Alto, CA10 decisions1981–19901 recall

FDA records 10 decisions for Collagen Corp. (Palo Alto, CA) from 1981 to 1990: 9 510(k) clearances and 1 original PMA approval. Most are in product codes DZE (Implant, Endosseous, Root-Form) and EFB (Handpiece, Air-Powered, Dental). 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 Collagen Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Collagen Corp. since 2007.

Recalls per year

1in 2015

2007high 1 (2015) · low 0 (2007)2026

Class I Class II/III not classified

FIG. 1 — Collagen 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 “Collagen”

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

Collagen Matrix, Inc. 47 Collagen Solutions, LLC 1

Collagen 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 “Collagen”