FDA applicant

Sterling Medical, Inc.

Goldsboro, NC1 decision2010–20100 recalls

FDA records 1 decision for Sterling Medical, Inc. (Goldsboro, NC) in 2010: 1 510(k) clearance. All are in product code LKF (Cannula, Manipulator/Injector, Uterine). 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 Medical, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2010

2010high 1 (2010) · low 0 (2011)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2010.

FIG. 1 — Sterling Medical, Inc. by year, 2010–2026Sources: 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 Multi-Products, Inc. 1

Sterling Medical, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Sterling”