FDA applicant

Neoligaments, Ltd.

Leeds, GB7 decisions1990–19950 recalls

FDA records 7 decisions for Neoligaments, Ltd. (Leeds, GB) from 1990 to 1995: 7 510(k) clearances. Most are in product codes JDR (Staple, Fixation, Bone) and HWE (Instrument, Surgical, Orthopedic, Ac-Powered…). 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, orthopedic panel, where it files most

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

FDA decisions per year

No FDA decision for Neoligaments, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Neoligaments, Ltd.

Which product codes does it file in?

What has FDA decided for it lately?