510(k) Report

FDA applicant

Loctite Corp.

Rocky Hill, CT1 decision1996–19960 recalls

FDA records 1 decision for Loctite Corp. (Rocky Hill, CT) in 1996: 1 510(k) clearance. All are in product code EMA (Cement, Dental). 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 Loctite Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Loctite Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Loctite Corp.’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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