510(k) Report

FDA applicant

Guangdong Ashmore Health Technology Co., Ltd.

Foshan, CN1 decision2026–20260 recalls

FDA records 1 decision for Guangdong Ashmore Health Technology Co., Ltd. (Foshan, CN) in 2026: 1 510(k) clearance. All are in product code OAP (Laser, Comb, Hair). 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, physical medicine panel, where it files most

How often FDA has decided Guangdong Ashmore Health Technology Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2026

2026 (partial year): 1
2026high 1 (2026)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2026.

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

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