FDA applicant

Westmark, Sterile Packing Systems, Inc. (Sps)

Grand Rapids, MI28 decisions1988–19900 recalls

FDA records 28 decisions for Westmark, Sterile Packing Systems, Inc. (Sps) (Grand Rapids, MI) from 1988 to 1990: 28 510(k) clearances. Most are in product codes GCX (Apparatus, Suction, Operating-Room, Wall…) and KOD (Catheter, Urological). 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 hospital panel, where it files most

How often FDA has decided Westmark, Sterile Packing Systems, Inc. (Sps)’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Westmark, Sterile Packing Systems, Inc. (Sps) since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Westmark, Sterile Packing Systems, Inc. (Sps) by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Westmark”

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

Westmark Hospital Supplies 7 Westmark Enterprises, Inc. 3 Westmark Sps, Inc. 1

Westmark, Sterile Packing Systems, Inc. (Sps)

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Westmark”