FDA applicant

Snyder Laboratories, Inc.

Mchenry, IL16 decisions1978–19840 recalls

FDA records 16 decisions for Snyder Laboratories, Inc. (Mchenry, IL) from 1978 to 1984: 16 510(k) clearances. Most are in product codes GCY (Apparatus, Suction, Single Patient Use…) and FCM (Tray, Catheterization, Sterile Urethral, With…). 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 Snyder Laboratories, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

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

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Snyder”

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

Snyder Industries, Inc. 1

Snyder Laboratories, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Snyder”