FDA applicant

Laser Endo Technic

San Clements, CA2 decisions1992–19920 recalls

FDA records 2 decisions for Laser Endo Technic (San Clements, CA) in 1992: 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 Laser Endo Technic’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Laser Endo Technic since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Laser Endo Technic’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 “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 Endo Technic

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Laser”