FDA applicant

Light Instrument, Ltd.

Binyamina, IL1 decision2006–20060 recalls

FDA records 1 decision for Light Instrument, Ltd. (Binyamina, IL) in 2006: 1 510(k) clearance. All are in product code GEX (Powered Laser Surgical Instrument). Its devices cite 2 predicates, 0 of them its own earlier devices. 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 Light Instrument, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Light Instrument, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Light Instrument, Ltd.’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 “Light”

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

Light Diagnostics 19 Light Tree Ventures Europe B.V. 13 Light Sources, Inc. 9 Light Age, Inc. 7 Light Instruments 2 Light-Med (Usa), Inc. 2 Light Force Therapy, Inc. 2 Light Bioscience, LLC 2 Light Relief, LLC 1 Light Guide Optics International, Ltd. 1 Light Technology Systems 1

Light Instrument, Ltd.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Light”