Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3007584446

FEI Number

3007584446

Entity Name

SHANGHAI SUPORE INSTRUMENTS CO. LTD.

City/State/Country

Shanghai, CN

Establishment Address

NO.800 Yeji road Baoshan District, Shanghai 200444, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Shanghai Supore Instruments Co. Ltd. (Owner Number: 10053340)

Owner / Operator Contact Address

NO.800 Yeji road Baoshan District, Shanghai, CN-SH 200444, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

SUPORE SUPORE

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HKO	Refractometer, Ophthalmic	Ophthalmic	Class 1	886.1760	2016-11-23
HKM	Retinoscope, Battery-Powered	Ophthalmic	Class 1	886.1780	2022-01-07

Official Correspondent

HONG YING GU

US Agent Details

Alejandro Kacheroff Business: BK frames CORP Email: alejandrok@bkframes.com Phone: (305) 6850001

Related Public Records

Same Entity

Shanghai Supore Instruments Co. Ltd.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007584446. Last updated year: 2026. Please use registration number 3007584446 when referencing this establishment in official correspondence.