FDA applicant

Sterling Multi-Products, Inc.

Walker, MI1 decision1984–19840 recalls

FDA records 1 decision for Sterling Multi-Products, Inc. (Walker, MI) in 1984: 1 510(k) clearance. All are in product code HTD (Forceps). 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 Sterling Multi-Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Sterling Multi-Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Sterling Multi-Products, 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 “Sterling”

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

Sterling Diagnostics, Inc. 41 Sterling Medivations, Inc. 27 Sterling Biochemical, Inc. 15 Sterling Drug, Inc. 9 Sterling Diagnostic Imaging, Inc. 7 Sterling Medical Devices, Inc. 2 Sterling U.S.A., Inc. 1 Sterling Medical, Inc. 1

Sterling Multi-Products, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Sterling”