FDA applicant

Lidco, Ltd.

London, GB7 decisions1999–20171 recall

FDA records 7 decisions for Lidco, Ltd. (London, GB) from 1999 to 2017: 7 510(k) clearances. All are in product code DXG (Computer, Diagnostic, Pre-Programmed…). Its devices cite 2 predicates, 0 of them its own earlier devices. 1 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, cardiovascular panel, where it files most

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

FDA decisions per year

1in 2017

2007high 2 (2013) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

1in 2020

2007high 1 (2020) · low 0 (2007)2026

Class I Class II/III not classified

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

Planning a device like Lidco, Ltd.’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

Lidco, 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?

What has been recalled?