FDA applicant

Applied Biomaterial Technologies

Silverdale, WA7 decisions1990–19950 recalls

FDA records 7 decisions for Applied Biomaterial Technologies (Silverdale, WA) from 1990 to 1995: 7 510(k) clearances. Most are in product codes FWP (Prosthesis, Chin, Internal) and MIB (Elastomer, Silicone Block). 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, general and plastic surgery panel, where it files most

How often FDA has decided Applied Biomaterial Technologies’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Applied Biomaterial Technologies since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Applied Biomaterial Technologies

Which product codes does it file in?

What has FDA decided for it lately?