510(k) Report

FDA applicant

Beijing Toplaser Technology Co., Ltd.

Chaoyang District, Beijing, CN3 decisions2014–20140 recalls

FDA records 3 decisions for Beijing Toplaser Technology Co., Ltd. (Chaoyang District, Beijing, CN) in 2014: 3 510(k) clearances. All are in product code GEX (Powered Laser Surgical Instrument). Its devices cite 6 predicates, 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 and plastic surgery panel, where it files most

How often FDA has decided Beijing Toplaser Technology Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

3in 2014

2014: 3
2014high 3 (2014) · low 0 (2015)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2014.

FIG. 1 — Beijing Toplaser Technology Co., Ltd. by year, 2014–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Beijing Toplaser Technology Co., Ltd.’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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