510(k) Report

FDA applicant

Clued UP Limited

Egham, Surrey, GB1 decision2003–20030 recalls

FDA records 1 decision for Clued UP Limited (Egham, Surrey, GB) in 2003: 1 510(k) clearance. All are in product code LPN (Accessories, Soft Lens Products). 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, ophthalmic panel, where it files most

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

FDA decisions per year

No FDA decision for Clued UP Limited since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Clued UP Limited’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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Which product codes does it file in?

  • LPNAccessories, Soft Lens Products1decision

What has FDA decided for it lately?

  • K030910Clued UP Multipurpose Solution- NO RubClued UP Limited · 2003

The one decision as Clued UP Limited →