510(k) Report

FDA applicant

R. Poon Medical Products Co., Ltd.

Hauppauge, NY1 decision2005–20050 recalls

FDA records 1 decision for R. Poon Medical Products Co., Ltd. (Hauppauge, NY) in 2005: 1 510(k) clearance. All are in product code IOR (Wheelchair, Mechanical). 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 R. Poon Medical Products Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for R. Poon Medical Products Co., Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — R. Poon Medical Products Co., Ltd. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like R. Poon Medical Products 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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