FDA applicant

Microaire Advanced Surgical Products

Valencia, CA2 decisions1991–19910 recalls

FDA records 2 decisions for Microaire Advanced Surgical Products (Valencia, CA) in 1991: 2 510(k) clearances. Most are in product codes EQH (Source, Carrier, Fiberoptic Light) and 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, ear, nose and throat panel, where it files most

How often FDA has decided Microaire Advanced Surgical Products’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Microaire Advanced Surgical Products since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Microaire Advanced Surgical Products’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 “Microaire”

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

Microaire Surgical Instruments, LLC 16 Microaire 3

Microaire Advanced Surgical Products

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Microaire”