510(k) Report

FDA applicant

Wuhan PHOMED Technology Company, Ltd.

Wuhan, CN2 decisions2026–20260 recalls

FDA records 2 decisions for Wuhan PHOMED Technology Company, Ltd. (Wuhan, CN) in 2026: 2 510(k) clearances. Most are in product codes ILY (Lamp, Infrared, Therapeutic Heating) and GEX (Powered Laser Surgical Instrument). Its devices cite 2 predicates, 0 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Wuhan Phomed Technology Co., Ltd.”.

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 Wuhan PHOMED Technology Company, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

2in 2026

2026 (partial year): 2
2026high 2 (2026)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2026.

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

Planning a device like Wuhan PHOMED Technology Company, 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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