BEUDAMED
    FDA Registration Active 🇨🇳 China

    GUANGZHOU XINBO ELECTRONIC CO., LTD

    Reg #: 3010097863 · FEI: 3010097863 · Expires 2026
    View on FDA
    Products
    18
    Proprietary Names
    50
    Establishment Types
    5
    Classifications
    18

    Registration Details

    Registration Name
    GUANGZHOU XINBO ELECTRONIC CO., LTD
    Registration Number
    3010097863
    FEI Number
    3010097863
    Status
    Active
    Expiry Year
    2026
    Initial Importer
    No
    Address
    23 Building, Phase-II Huachuang Industry Park, Panyu
    City
    guangzhou Guangdong
    Country
    CN

    Regulatory Submissions

    510(k) Number
    K151693

    Owner / Operator

    Firm Name
    Guangzhou Xinbo Electronic Co., Ltd
    Operator Number
    10056647
    Address
    23 Building, Phase -II Huachuang Industry Park, Panyu
    City
    guangzhou
    State
    Guangdong
    Postal Code
    511450
    Country
    CN
    Correspondent
    Huifang Li

    US Agent

    Business Name
    Pro Pharma Group
    Contact Name
    Cherita James
    Address
    1129 20th St Nw Ste 600
    City
    Washington
    State
    DC
    ZIP
    20036
    Country
    US
    Email
    [email protected]
    Phone
    347 9540624

    Products

    Device Name Product Code
    Electrode, Cutaneous GXY
    Stimulator, Electrical, Transcutaneous, For Arthritis NYN
    Stimulator, Muscle, Powered IPF
    Stimulator, Nerve, Transcutaneous, Over-The-Counter NUH
    Stimulator, Nerve, Transcutaneous, For Pain Relief GZJ
    Stimulator, Muscle, Powered, For Muscle Conditioning NGX
    Orthosis, Corrective Shoe KNP
    Component, Traction, Non-Invasive KQZ
    Apparatus, Traction, Non-Powered HST
    Orthosis, Moldable, Supportive, Skin Protective MNE
    Media, Electroconductive GYB
    Orthosis, Cervical IQK
    Pad, Heating, Powered IRT
    Massager, Therapeutic, Electric ISA
    Pack, Hot Or Cold, Disposable IMD
    Orthosis, Lumbar IQE
    Orthosis, Limb Brace IQI
    Cushion, Wheelchair IMP

    Proprietary Names

    DR-HO's Foot Pad Electrode Pain Therapy Device (Model: P.T.S.-Vi, P.T.S.-Vii) DR-HO's Air Orthotics Diabetic Insoles DR-HO's Neck Comforter Neck Comforter Dr-Ho's Foot Pad Electrode (Models: DHFRE-I, CP-I, CP-II, CP-III) Equate Pain Therapy Neck Pain Pro Circulation Promoter Pain Relief System Pain Therapy 4-Pad Pain Therapy DH-PTS-I, DH-PTS-II, DH-PTS-IIA, DH-PTS-IIB, DH-CP-I Pain Therapy System Models: P.T.S-III Decompression Belt DR-HO's Decompression Belt HoPhysio Belt DR-HO'S Knee Compression Support(NN-KN-Blue) DR-HO'S Elbow Compression Support(NN-EL-Blue) DR-HO'S Shoulder Support(NN-SH-Blue) DR-HO'S Calf Compression Support(NN-CA-Blue) DR-HO'S Back Support Belt(NN-LB-Black) DR-HO'S Wrist & Hand Compression Support(NN-WR-Blue) DR-HO'S Ankle Compression Support(NN-AN-Blue) Cutaneous Electrode XinBo Electrodes DR-HO's Neck Pain Pro Fabric Electrodes Electro-Therapy Conductive Gel DR-HO'S Adjustable Pillow Back Pain Relief System Pro Leg Circulation Promoter Blocks with Electrode, Leg Circulation Promoter Cushion with Electrode, Elbow and Wrist Therapy Support with Electrodes, Knee and Calf Muscle Support with Electrodes, All Day Pain Relief Shirt Thigh Muscle Support with Electrodes Knee support with Air Compression and Electrodes, Triple Action Back Belt with Dual Support Bands, Air Compression and E Pain Therapy Belt with Electrodes MotionCiser MotionCiser Exercise Bands DR-HO's Heat Therapy Belt Magic Heat Pad DR-HO's Perfect Back Rest DR-HO's Back Support Belt Conductive Silicone Rubber Electrode Pain Therapy Device (Model: P.TS.-X) Triple Action Back Belt with Dual Support Bands and Adjustable Air Compression,Knee Support with Air Compression DR-HO's Shoulder Support, DR-HO's Wrist Support, DR-HO's Elbow Compression Support, DR-HO's Knee Compression Support, DR-HO's Ankle Compression Support, DR-HO's Foot and Ankle Compression support DR-HO's Calf Compression Support Conductive Carbon Film Electrode Air Wave Cushion

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer) Manufacture Medical Device Foreign Private Label Distributor Complaint File Establishment per 21 CFR 820.198 Repack or Relabel Medical Device