FDA applicant

Lasag Medical Lasers

Eden Prairie, MN2 decisions1989–19900 recalls

FDA records 2 decisions for Lasag Medical Lasers (Eden Prairie, MN) from 1989 to 1990: 2 510(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 Lasag Medical Lasers’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Lasag Medical Lasers since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Lasag Medical Lasers’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 “Lasag”

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

Lasag AG 2

Lasag Medical Lasers

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Lasag”