FDA applicant

Arthrex Arthroscopy Instruments, Inc.

Norwalk, CT2 decisions1988–19880 recalls

FDA records 2 decisions for Arthrex Arthroscopy Instruments, Inc. (Norwalk, CT) in 1988: 2 510(k) clearances. All are in product code HRX (Arthroscope). 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 Arthrex Arthroscopy Instruments, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Arthrex Arthroscopy Instruments, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Arthrex Arthroscopy Instruments, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Arthrex Arthroscopy Instruments, Inc.’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 “Arthrex”

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

Arthrex, Inc. 355

Arthrex Arthroscopy Instruments, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Arthrex”