FDA applicant

Schmid Laboratories, Inc.

Little Falls, NJ10 decisions1980–19900 recalls

FDA records 10 decisions for Schmid Laboratories, Inc. (Little Falls, NJ) from 1980 to 1990: 10 510(k) clearances. All are in product code HIS (Condom). 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, obstetrics and gynecology panel, where it files most

How often FDA has decided Schmid Laboratories, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Schmid Laboratories, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Schmid Laboratories, Inc.

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?