510(k) Report

FDA applicant

Forum Engineering Technologies, Ltd.

Rishon Lezion, IL1 decision2013–20130 recalls

FDA records 1 decision for Forum Engineering Technologies, Ltd. (Rishon Lezion, IL) in 2013: 1 510(k) clearance. All are in product code LQY (Locator, Root Apex). Its devices cite 1 predicate, 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

How often FDA has decided Forum Engineering Technologies, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2013

2013: 1
2013high 1 (2013) · low 0 (2014)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2013.

FIG. 1 — Forum Engineering Technologies, Ltd. by year, 2013–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Forum Engineering Technologies, 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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Other applicant names beginning “Forum”

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