FDA applicant

Minnesota Laser Corp.

Minneapolis, MN12 decisions1985–19880 recalls

FDA records 12 decisions for Minnesota Laser Corp. (Minneapolis, MN) from 1985 to 1988: 12 510(k) clearances. Most are in product codes GEX (Powered Laser Surgical Instrument) and HHR (Laser, Surgical, Gynecologic). 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 Minnesota Laser Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Minnesota Laser Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Minnesota Laser Corp.’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 “Minnesota”

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

Minnesota Mining and Mfg. Co. 9 Minnesota Scientific, Inc. 5 Minnesota Valley Engineering, Inc. 4 Minnesota Medical Development, Inc. 3 Minnesota Prophy Power, Inc. 2 Minnesota Resuscitation Solutions, D.B.D Advancedcpr… 1 Minnesota Medical Technologies 1 The Minnesota Back Brace Co. 1

Minnesota Laser Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Minnesota”