ZUMAX MEDICAL CO, LTD.

FDA Device Registration & Listing · SUZHOU,JIANGSU, CN · Registration 3006252153

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3006252153
FEI Number
3006252153
Entity Name
ZUMAX MEDICAL CO, LTD.
City/State/Country
SUZHOU,JIANGSU, CN
Establishment Address
5 ZHIYING STREET, SUZHOU NEW DISTRICT, SUZHOU,JIANGSU 215129, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
ZUMAX MEDICAL CO, LTD. (Owner Number: 9093892)
Owner / Operator Contact Address
5 ZHIYING STREET, SUZHOU NEW DISTRICT, SUZHOU, CN-JS 215129, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

DSD-01 Dental Suction Unit DM6F Ophthalmoscope DM6GP Ophthalmoscope DM6G Ophthalmoscope DM6FP Ophthalmoscope DW3010 DW1050 DW1100 DW1000 DW3060 DW2010 DW1060 CLS3080 Colposcope SR24B STREAK RETINOSCOPES SR24A STREAK RETINOSCOPES DW3050 SR24 STREAK RETINOSCOPES GL50 Series Illuminator 472E0010 GL60 Series Illuminator 485 0010 4057850 411E0010 405E7850 4677860 490-0015 DM6UEP 4110010 487 1000 488 1000 DM6DP DM6U DM6UE 410E0010 410-0010 DW2000 DM6UP DM6C 467E7860 DM6DEP DM6D DM6BE DW3000 489 0010 DM6BEP DM6DE DM6CE BM800 Binocular Indirect Ophthalmoscope SL200 Handheld slit lamp SL260 slit lamp VARIOUS MODELS BINOCULAR LOUPES SLT Binocular Loupes SLE Binocular Loupes SLH Binocular Loupes SLF Binocular Loupes SLD Binocular Loupes SLS Binocular Loupes DFK Binocular Loupes DFK air Binocular Loupes DFT Binocular Loupes SLK Binocular Loupes

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EBR Unit, Suction Operatory Dental Class 1 872.6640 2024-12-03
HLI Ophthalmoscope, Ac-Powered Ophthalmic Class 2 886.1570 2017-08-16
PTZ Colposcope (And Colpomicroscope), Exempt Obstetrics/Gynecology Class 2 884.1630 2024-01-15
HKM Retinoscope, Battery-Powered Ophthalmic Class 1 886.1780 2006-10-31
HJN Transilluminator, Battery-Powered Ophthalmic Class 1 886.1945 2019-04-10
KYT Light, Examination, Medical, Battery Powered General Hospital Class 1 880.6350 2017-03-13
HLJ Ophthalmoscope, Battery-Powered Ophthalmic Class 2 886.1570 2016-04-26
PUE Biomicroscope, Slit-Lamp, Ac-Powered, Exempt Ophthalmic Class 2 886.1850 2019-04-09
HLI Ophthalmoscope, Ac-Powered Ophthalmic Class 2 886.1570 2016-09-12
KZF Device, Medical Examination, Ac Powered General Hospital Class 1 880.6320 2017-03-13
EPY Speculum, Ent General, Plastic Surgery Class 1 878.1800 2016-08-10
HJH Loupe, Binocular, Low Power Ophthalmic Class 1 886.5120 2006-10-24

Official Correspondent

XIANGDONG LI

US Agent Details

Grace Wei Business: Zumax USA, Inc. Email: grace.wei@zumaxmedical.com Phone: (651) 3003907

Related Public Records

Same Entity

ZUMAX MEDICAL CO, LTD.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K142953 Optomedical Technologies GmbH OCT-Camera 2015-03-04
K851742 Burton Medical Products Corp. MEDICAL EXAMINATION LIGHTS 1985-05-13
K834189 Imm Enterprises , Ltd. JAKOBI SURG. INSTRUMENTS #7 44/47 1984-03-06

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0008-2018 Optovue, Inc. 2
iVue with Normative Database, Device Listing Number D185549. Product Usage: The iVue (K121739) is a non-contact, high resolution tomographic imaging device. It is intended for in vivo imaging, axial cross-sectional, and three dimensional imaging and measurement of anterior and posterior ocular structures, including retina, retinal nerve fiber layer, ganglion cell complex (GCC), optic disc, cornea, and anterior chamber of the eye. The iVue with Normative Database is a quantitative tool for the comparison of retina, retinal nerve fiber layer, ganglion cell complex, and optic disc measurements to a database of known normal subjects. The iVue with Normative Database is indicated for use as a device to aid in the diagnosis, documentation, and management of ocular health and diseases in the adult population.
Z-0010-2018 Optovue, Inc. 2
iVue 500 with iScan, D216606. Product non-contact, high resolution tomographic imaging device. It is intended for in vivo imaging, axial cross-sectional and three-dimensional imaging and measurement of anterior and posterior ocular structures, including retina, retinal nerve fiber layer, ganglion cell complex (GCC), optic disc, cornea, and anterior chamber of the eye. The iVue 500 with normative database is a quantitative tool for the comparison of retina, retinal nerve fiber layer, ganglion cell complex, and optic disc measurements to a database of known normal subjects. The iVue 500 with normative database is indicated for use as a device to aid in the diagnosis, documentation, and management of ocular health and diseases in the adult population.

Similar Registrations

Registration Number Establishment Name Location
3043648115 DEBO MEDICAL TECHNOLOGY (SHIJIAZHUANG) CO., LTD. Shijiazhuang Hebei, CN
3017181414 JIANGSU YONGFA MEDICAL EQUIPMENT TECHNOLOGY CO., LTD Zhangjiagang City Jiangsu, CN
3019103 BEAVERSTATE DENTAL, INC. NEWBERG, OR, US
3010373263 JIANGSU SAIKANG MEDICAL EQUIPMENT CO., LTD Zhangjiagang Jiangsu, CN
3008770655 BEYES DENTAL INC Toronto Ontario, CA
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3006252153. Last updated year: 2026. Please use registration number 3006252153 when referencing this establishment in official correspondence.
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