510(k) Report

FDA applicant

Microaire

Valencia, CA3 decisions1991–19920 recalls

FDA records 3 decisions for Microaire (Valencia, CA) from 1991 to 1992: 3 510(k) clearances. Most are in product codes HRX (Arthroscope) and GEF (Applier, Staple, Surgical,). 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 Microaire’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Microaire since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Microaire”

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