Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3043729153

FEI Number

3043729153

Entity Name

BEIJING HOME VISION AI TECH CO.,LTD.

City/State/Country

Beijing, CN

Establishment Address

Room 222, 2nd Floor, Chuanyan Building, No A7 Jiaomen Road, Fengtai District, Beijing 100068, CN

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility,Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device

Owner / Operator

Beijing Home Vision AI Tech Co.,Ltd. (Owner Number: 10095190)

Owner / Operator Contact Address

Room 222, 2nd Floor, Chuanyan Building, No A7 Jiaomen Road, Fengtai District, Beijing, CN-BJ 100068, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Refractometer HVK10 Refractometer HVR10 Home Vision Screener HVS10 Home Vision Screener C10 Home Vision Screener H10

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HKO	Refractometer, Ophthalmic	Ophthalmic	Class 1	886.1760	2026-02-04

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp Email: David.Lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

Beijing Home Vision AI Tech 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 3043729153. Last updated year: 2026. Please use registration number 3043729153 when referencing this establishment in official correspondence.