FDA applicant

Forum Engineering Technologies (96), Ltd.

Ashkelon, IL2 decisions2011–20240 recalls

FDA records 2 decisions for Forum Engineering Technologies (96), Ltd. (Ashkelon, IL) from 2011 to 2024: 2 510(k) clearances. Most are in product codes EKX (Handpiece, Direct Drive, Ac-Powered) and 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

FIG. A — Illustration, dental panel, where it files most

How often FDA has decided Forum Engineering Technologies (96), Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2024

2011high 1 (2011) · low 0 (2012)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2011.

FIG. 1 — Forum Engineering Technologies (96), Ltd. by year, 2011–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Forum Engineering Technologies (96)…’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.

Forum Engineering Technologies, Ltd. 1

Forum Engineering Technologies (96), 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 “Forum”