510(k) Report

FDA applicant

Ximex, Ltd.

England Sw13 9nt, GB1 decision1989–19890 recalls

FDA records 1 decision for Ximex, Ltd. (England Sw13 9nt, GB) in 1989: 1 510(k) clearance. All are in product code JET (Pick, Massaging). 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 Ximex, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ximex, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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