FDA applicant

Stirn Industries

Dayton, NJ3 decisions1991–19920 recalls

FDA records 3 decisions for Stirn Industries (Dayton, NJ) from 1991 to 1992: 3 510(k) clearances. Most are in product codes JCX (Apparatus, Suction, Ward Use, Portable…) and FLE (Sterilizer, Steam). 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 Stirn Industries’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Stirn Industries since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Stirn Industries

Which product codes does it file in?

What has FDA decided for it lately?