510(k) Report

FDA applicant

Imprint Pharmaceuticals Limited

East Molesey, Surrey, GB2 decisions2005–20060 recalls

FDA records 2 decisions for Imprint Pharmaceuticals Limited (East Molesey, Surrey, GB) from 2005 to 2006: 2 510(k) clearances. All are in product code FMI (Needle, Hypodermic, Single Lumen). 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, general hospital panel, where it files most

How often FDA has decided Imprint Pharmaceuticals Limited’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Imprint Pharmaceuticals Limited since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Imprint Pharmaceuticals Limited’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report