FDA applicant

Mcgrath Surgical, Ltd.

Po3 5hl England, GB1 decision1990–19900 recalls

FDA records 1 decision for Mcgrath Surgical, Ltd. (Po3 5hl England, GB) in 1990: 1 510(k) clearance. All are in product code HWC (Screw, Fixation, Bone). 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, orthopedic panel, where it files most

How often FDA has decided Mcgrath Surgical, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Mcgrath Surgical, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Mcgrath”

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

Mcgrath Pharmaceuticals, Inc. 1

Mcgrath Surgical, Ltd.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Mcgrath”