FDA applicant
Anhui Jbh Medical Apparatus Co., Ltd.
FDA records 14 decisions for Anhui Jbh Medical Apparatus Co., Ltd. (Chuzhou, CN) from 2021 to 2026: 14 510(k) clearances. Most are in product codes ITI (Wheelchair, Powered) and INI (Vehicle, Motorized 3-Wheeled). Since 2016 its 510(k)s took a median of 163 days from receipt to decision, against 108 for FDA’s reviews in the same codes and years. Its devices cite 10 predicates, 4 of them its own earlier devices. No recall is linked to its devices.
FDA’s records also spell it “Anhui JBH Medical Apparatus Co., Ltd.”.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Anhui Jbh Medical Apparatus Co., Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
3in 2025
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2021.
Planning a device like Anhui Jbh Medical Apparatus Co., Ltd.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) Report