Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3020410096

FEI Number

3020410096

Entity Name

MAIN MEDITECH CO., LTD

City/State/Country

Chongqing, CN

Establishment Address

Unit 4-2, No. 56, HuJu Road, YuZhong District, Chongqing 400010, CN

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device

Owner / Operator

Main MediTech Co., Ltd (Owner Number: 10083983)

Owner / Operator Contact Address

Unit 4-2, No. 56, HuJu Road, YuZhong District, Chongqing, CN-CQ 400010, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Main MediTech Ophthalmic tables Peirmeter SVF-6000,SVF-7000,SVF-9000 Fundus Camera SFC-1000,SFC-2000

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HRK	Table, Instrument, Manual, Ophthalmic	Ophthalmic	Class 1	886.4855	2022-06-06
HPT	Perimeter, Automatic, Ac-Powered	Ophthalmic	Class 1	886.1605	2022-01-05
PJZ	Camera, Ophthalmic, General-Use	Ophthalmic	Class 2	886.1120	2022-01-05

Official Correspondent

Joy Tse

US Agent Details

FANFEI LIU Email: U.S.agent@frosatechnology.com Phone: (626) 8261385

Related Public Records

Same Entity

Main MediTech 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 3020410096. Last updated year: 2026. Please use registration number 3020410096 when referencing this establishment in official correspondence.