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Data / Medical devices / China / Anhui JBH Medical Apparatus Co., Ltd

Anhui JBH Medical Apparatus Co., Ltd: FDA-registered device maker in Chuzhou Anhui, China, 15 510(k) clearances

Anhui JBH Medical Apparatus Co., Ltd is registered with the FDA (registration 3016969129) in Chuzhou Anhui, China. It lists 5 device types. The FDA files 15 510(k) clearances under its listings, the newest dated October 14, 2026. Registered through 2027. FDA data exported November 3, 2026.

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FDA registration number
3016969129
Address
No.116QiCang Road Industrial Distric MingGuang, Chuzhou Anhui, China, 239400
Owner or operator
Anhui JBH Medical Apparatus Co., Ltd (10083603)
Roles
Exporter to the US, Manufacturer
First device listed
December 5, 2021
Registered through
2027
Brand names listed
Electric Scooter (FBC01), Electric Scooters: FDB08/FDB08A/FDB12, Electric Scooters: FNS01/FNS03, Electric wheelchair: D39, Electric wheelchair: DC12, Knee walker; WALKER, MECHANICAL, Manual Wheelchair (Models S002, S004, S005, S006, S007, S008, S009), PATIENT LIFT and more

Devices it lists

DeviceProduct codeClassRoleSource
Lift, Patient, Ac-PoweredFNG2Exporter to the US, Manufactureraccessdata.fda.gov
Vehicle, Motorized 3-WheeledINI2Exporter to the US, Manufactureraccessdata.fda.gov
Walker, MechanicalITJ1Exporter to the US, Manufactureraccessdata.fda.gov
Wheelchair, MechanicalIOR1Exporter to the US, Manufactureraccessdata.fda.gov
Wheelchair, PoweredITI2Exporter to the US, Manufactureraccessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
October 14, 2026K261169Power Wheelchair (D39)ITISubstantially EquivalentAnhui JBH Medical Apparatus Co., Ltd.accessdata.fda.gov
October 6, 2026K261200Power Wheelchair (D60)ITISubstantially EquivalentAnhui JBH Medical Apparatus Co., Ltd.accessdata.fda.gov
October 6, 2026K261079Power Wheelchair (DC12)ITISubstantially EquivalentAnhui JBH Medical Apparatus Co., Ltd.accessdata.fda.gov
September 24, 2026K261078Electric Scooter (FNS01,FNS03)INISubstantially EquivalentAnhui Jbh Medical Apparatus Co., Ltd.accessdata.fda.gov
September 19, 2026K261859Electric Scooter (FDB08, FDB08A, FDB12)INISubstantially EquivalentAnhui JBH Medical Apparatus Co., Ltd.accessdata.fda.gov
June 25, 2025K251606Power Wheelchair (D26)ITISubstantially EquivalentAnhui Jbh Medical Apparatus Co., Ltd.accessdata.fda.gov
February 28, 2025K241374Manual Wheelchair (S002, S004, S005, S006, S007, S008, S009)IORSubstantially EquivalentAnhui Jbh Medical Apparatus Co., Ltd.accessdata.fda.gov
January 2, 2025K242448Power Wheelchair (D03, D05, D06, D09, D11, D16, D22, D23, D26, D36)ITISubstantially EquivalentAnhui Jbh Medical Apparatus Co., Ltd.accessdata.fda.gov
December 31, 2024K242468Power Wheelchair (D10, D12, D15, D17, D20, D37)ITISubstantially EquivalentAnhui Jbh Medical Apparatus Co., Ltd.accessdata.fda.gov
December 27, 2024K242252Power WheelchairITISubstantially EquivalentAnhui Jbh Medical Apparatus Co., Ltd.accessdata.fda.gov
October 4, 2024K241854Power WheelchairITISubstantially EquivalentAnhui Jbh Medical Apparatus Co., Ltd.accessdata.fda.gov
May 6, 2022K212092Portable Folding Electric Wheelchair (Model: DC01)ITISubstantially EquivalentAnhui Jbh Medical Apparatus Co., Ltd.accessdata.fda.gov
April 22, 2022K212090Electric ScooterINISubstantially EquivalentAnhui Jbh Medical Apparatus Co., Ltd.accessdata.fda.gov
June 25, 2021K201196Scooter (Model: FDB01)INISubstantially EquivalentNanjing Jin Bai HE Medical Apparatus Co., Ltd.accessdata.fda.gov
August 9, 2017K170787Powered Wheelchair DYW30A(D09)ITISubstantially EquivalentNanjing Jin Bai HE Medical Apparatus Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated October 14, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.