FDA applicant

Laser Industries of Tel Aviv

Mchenry, IL1 decision1982–19820 recalls

FDA records 1 decision for Laser Industries of Tel Aviv (Mchenry, IL) in 1982: 1 510(k) clearance. All are in product code EOQ (Bronchoscope (Flexible Or Rigid)). 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, ear, nose and throat panel, where it files most

How often FDA has decided Laser Industries of Tel Aviv’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Laser Industries of Tel Aviv since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Laser Industries of Tel Aviv’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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 Industries of Tel Aviv

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?

Other applicant names beginning “Laser”