FDA applicant

Laser Technologies Group, Inc.

Edina, MN1 decision1989–19893 recalls

FDA records 1 decision for Laser Technologies Group, Inc. (Edina, MN) in 1989: 1 510(k) clearance. All are in product code FYD (Apparatus, Exhaust, Surgical). 3 recalls are 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 Laser Technologies Group, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Laser Technologies Group, Inc. since 2007.

Recalls per year

3in 2026

2007high 3 (2026) · low 0 (2007)2026

Class I Class II/III not classified

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

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See the 510(k) Report

Other applicant names beginning “Laser”

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

Laser Industries, Ltd. 20 Laser Engineering, Inc. 18 L.A.S.E.R., Inc. 14 Laser Photonics, Inc. 14 Laser Media 13 Laser Peripherals, LLC 12 Laser-Optik-Systeme GmbH & Co. KG 7 Laser Spectrum, Inc. 5 Laser Max Medical Technologies Corp. 4 Laser Surgical Systems 3 Laser Associated Sciences, Inc. 2 Laser Dental Innovations 2

Laser Technologies Group, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

What has been recalled?

Other applicant names beginning “Laser”