FDA applicant

Sterling U.S.A., Inc.

Bristol, CT1 decision1995–19950 recalls

FDA records 1 decision for Sterling U.S.A., Inc. (Bristol, CT) in 1995: 1 510(k) clearance. All are in product code HHD (Pad, Menstrual, Unscented). 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 Sterling U.S.A., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Sterling U.S.A., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Sterling U.S.A., 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 Medical, Inc. 1 Sterling Multi-Products, Inc. 1

Sterling U.S.A., Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Sterling”