FDA applicant

Lasermed, Inc.

Salt Lake City, UT7 decisions1983–19990 recalls

FDA records 7 decisions for Lasermed, Inc. (Salt Lake City, UT) from 1983 to 1999: 7 510(k) clearances. Most are in product codes GEX (Powered Laser Surgical Instrument) and HQE (Instrument, Vitreous Aspiration And Cutting…). No recall is linked to its devices.

FDA’s records also spell it “Lasermed Corp.”, “Lasermed”.

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 Lasermed, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Lasermed, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Lasermed, 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?