SHANGHAI LINK INSTRUMENTS CO.,LTD

FDA Device Registration & Listing · Changzhou City Jiangsu, CN · Registration 3010774780

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
3010774780
FEI Number
3010774780
Entity Name
SHANGHAI LINK INSTRUMENTS CO.,LTD
City/State/Country
Changzhou City Jiangsu, CN
Establishment Address
5th Floor, Building 1, No. 17, Beitanghe East Road, Tianning District, Changzhou City Jiangsu 213000, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
SHANGHAI LINK INSTRUMENTS CO.,LTD (Owner Number: 10053961)
Owner / Operator Contact Address
5th Floor, Building 1, No. 17, Beitanghe East Road, Tianning District, Changzhou City, CN-JS 213000, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Auto lensmeter Perimeter Trial lens set Phoropter Frame Heater; Auto Lens Edger Operation Microscope Auto refractometer, Vision Screener Ophthalmic instrument table, Ophthalmic Chair and Stand Unit PD Meter Thermometer Face Mask Face Mask Optical Coherence Tomography, Ophthalmoscope Face Mask Otoscope, Otoscope Wall Mount System Smart Glasses

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HLM Instrument, Measuring, Lens, Ac-Powered Ophthalmic Class 1 886.1425 2019-02-09
HOO Perimeter, Ac-Powered Ophthalmic Class 1 886.1605 2019-12-17
HPC Set, Lens, Trial, Ophthalmic Ophthalmic Class 1 886.1405 2019-12-17
HKN Refractor, Manual, Non-Powered, Including Phoropter Ophthalmic Class 1 886.1770 2019-02-09
HLF Device, Measuring, Lens Radius, Ophthalmic Ophthalmic Class 1 886.1430 2021-12-24
HRM Microscope, Operating & Accessories, Ac-Powered, Ophthalmic General, Plastic Surgery Class 1 878.4700 2019-12-17
HKO Refractometer, Ophthalmic Ophthalmic Class 1 886.1760 2019-02-09
HRJ Table, Instrument, Powered, Ophthalmic Ophthalmic Class 1 886.4855 2017-01-31
HLH Pupillometer, Manual Ophthalmic Class 1 886.1700 2019-02-09
PXH Thermometer Kit General Hospital Class 2 880.2910 2020-03-23
LYU Accessory, Surgical Apparel General, Plastic Surgery Class 1 878.4040 2020-03-23
QKR Face Mask Within The Scope Of The Face Mask And Barrier Face Covering Enforcement Policy Or Face Mask Umbrella Eua Unknown Class N N/A 2020-05-20
HLI Ophthalmoscope, Ac-Powered Ophthalmic Class 2 886.1570 2024-04-09
FXO Suit, Surgical General, Plastic Surgery Class 1 878.4040 2020-03-23
ERA Otoscope Ear, Nose, Throat Class 1 874.4770 2024-08-26
HQY Sunglasses (Non-Prescription Including Photosensitive) Ophthalmic Class 1 886.5850 2025-03-06

Official Correspondent

Xiaoli Sun

US Agent Details

Leeyeo Kee Business: Regrek LLC Email: regrek.cs@hotmail.com Phone: (302) 6089028

Related Public Records

Same Entity

SHANGHAI LINK INSTRUMENTS 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
K900478 Woodlyn, Inc. WOODLYN FULL APERTURE TRIAL LENS SET 1990-02-21
K142953 Optomedical Technologies GmbH OCT-Camera 2015-03-04
K932506 Rudolf Riester GmbH & Co. KG RI-SCOPE (S) 1993-10-08
K940726 Jay-Y Enterprises Co., Inc. NONE-GENERIC 1994-04-11
K934837 Simon Marketing, Inc. SUNGLASSES 1993-12-08

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.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010774780. Last updated year: 2026. Please use registration number 3010774780 when referencing this establishment in official correspondence.
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