FDA applicant

Medical Device Services

St. George, UT6 decisions2002–20020 recalls

FDA records 6 decisions for Medical Device Services (St. George, UT) in 2002: 6 510(k) clearances. Most are in product codes JOW (Sleeve, Limb, Compressible) and HWE (Instrument, Surgical, Orthopedic, Ac-Powered…). Its devices cite 3 predicates, 0 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Medical Device Services, Inc.”.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, cardiovascular panel, where it files most

How often FDA has decided Medical Device Services’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medical Device Services since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Medical Device Services

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?