Anhui Jbh Medical Apparatus Co., Ltd.

FDA Regulatory Profile

Anhui Jbh Medical Apparatus Co., Ltd. appears in FDA public data with 0 recalls, 10 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on September 19, 2026.

Summary

Total Recalls
0
510(k) Clearances
10
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K261859Electric Scooter (FDB08, FDB08A, FDB12)September 19, 2026
K251606Power Wheelchair (D26)June 25, 2025
K241374Manual Wheelchair (S002, S004, S005, S006, S007, S008, S009)February 28, 2025
K242448Power Wheelchair (D03, D05, D06, D09, D11, D16, D22, D23, D26, D36)January 2, 2025
K242468Power Wheelchair (D10, D12, D15, D17, D20, D37)December 31, 2024
K242252Power WheelchairDecember 27, 2024
K241854Power WheelchairOctober 4, 2024
K212092Portable Folding Electric Wheelchair (Model: DC01)May 6, 2022
K212090Electric ScooterApril 22, 2022
K210302Disposable Medical maskMay 14, 2021