510(k) Report

FDA applicant

Lccs Products Limited

Hong Kong, CN5 decisions2011–20200 recalls

FDA records 5 decisions for Lccs Products Limited (Hong Kong, CN) from 2011 to 2020: 5 510(k) clearances. Most are in product codes GXI (Probe, Radiofrequency Lesion) and GEI (Electrosurgical, Cutting & Coagulation &…). Its devices cite 7 predicates, 1 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, neurology panel, where it files most

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

FDA decisions per year

1in 2020

2011: 12013: 22016: 12020: 1
2011high 2 (2013) · low 0 (2012)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2011.

FIG. 1 — Lccs Products Limited by year, 2011–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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