Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3013072273

FEI Number

3013072273

Entity Name

VIVO OPTICS CO., LTD

City/State/Country

Shanghai, CN

Establishment Address

Room 502-504,Block B,Central Tower, No. 567 Langao Road , Putuo District, Shanghai 200061, CN

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer),Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device

Owner / Operator

VIVO OPTICS CO., LTD (Owner Number: 10050758)

Owner / Operator Contact Address

Room 502-504,Block B,Central Tower, No. 567 Langao Road, Putuo District, Shanghai, CN-SH 200061, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Frame spectacle

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HQZ	Frame, Spectacle	Ophthalmic	Class 1	886.5842	2019-07-26

Official Correspondent

Mandy Xu

US Agent Details

James H. Liao Email: james@sino2us.com Phone: (310) 3758169

Related Public Records

Same Entity

VIVO OPTICS 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
K910951	United Optical, Spa	OPTHLAMIC FRAMES	1991-05-06

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3009554831	ROGER EYE DESIGN	Etten-Leur Noord-Brabant, NL
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013072273. Last updated year: 2026. Please use registration number 3013072273 when referencing this establishment in official correspondence.