510(k) Report

FDA applicant

Esc Medical Systems, Ltd.

Yokneam, IL13 decisions1996–20000 recalls

FDA records 13 decisions for Esc Medical Systems, Ltd. (Yokneam, IL) from 1996 to 2000: 13 510(k) clearances. All are in product code GEX (Powered Laser Surgical Instrument). Its devices cite 22 predicates, 5 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Esc Medical Systems, Inc.”.

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 Esc Medical Systems, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Esc Medical Systems, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Esc Medical Systems, Ltd.’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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