FDA applicant

Microquartz Medical, Inc.

Phoenix, AZ6 decisions1995–19960 recalls

FDA records 6 decisions for Microquartz Medical, Inc. (Phoenix, AZ) from 1995 to 1996: 6 510(k) clearances. All are in product code GEX (Powered Laser Surgical Instrument). 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, general and plastic surgery panel, where it files most

How often FDA has decided Microquartz Medical, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Microquartz Medical, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Microquartz Medical, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?