FDA applicant

Sterling Drug, Inc.

Mchenry, IL9 decisions1978–19900 recalls

FDA records 9 decisions for Sterling Drug, Inc. (Mchenry, IL) from 1978 to 1990: 9 510(k) clearances. Most are in product codes LYC (Bone Grafting Material, Synthetic) and KGN (Wound Dressing With Animal-Derived Material (S)). 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, dental panel, where it files most

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

FDA decisions per year

No FDA decision for Sterling Drug, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Sterling Drug, 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 Diagnostic Imaging, Inc. 7 Sterling Medical Devices, Inc. 2 Sterling U.S.A., Inc. 1 Sterling Medical, Inc. 1 Sterling Multi-Products, Inc. 1

Sterling Drug, 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?

Other applicant names beginning “Sterling”