FDA applicant

McGinley Orthopaedic Innovations

Casper, WY1 decision2026–20260 recalls

FDA records 1 decision for McGinley Orthopaedic Innovations (Casper, WY) in 2026: 1 510(k) clearance. All are in product code HSB (Rod, Fixation, Intramedullary And Accessories). 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 McGinley Orthopaedic Innovations’s devices, and how often a recall has named them.

FDA decisions per year

1in 2026

2026high 1 (2026)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2026.

FIG. 1 — McGinley Orthopaedic Innovations by year, 2026–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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

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Other applicant names beginning “McGinley”

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

Mcginley Innovations 1 Mcginley Orthpaedic Innovations, LLC 1

McGinley Orthopaedic Innovations

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “McGinley”