FDA applicant

Westmark Hospital Supplies

Grand Rapids, MI7 decisions1992–19930 recalls

FDA records 7 decisions for Westmark Hospital Supplies (Grand Rapids, MI) from 1992 to 1993: 7 510(k) clearances. Most are in product codes LRO (General Surgery Tray) and GEI (Electrosurgical, Cutting & Coagulation &…). 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 Westmark Hospital Supplies’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Westmark Hospital Supplies since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Westmark Hospital Supplies’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Westmark”

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

Westmark, Sterile Packing Systems, Inc. (Sps) 28 Westmark Enterprises, Inc. 3 Westmark Sps, Inc. 1

Westmark Hospital Supplies

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Westmark”