Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3043656118

FEI Number

3043656118

Entity Name

SHENZHEN XINGYI INTELLIGENT TECHNOLOGY CO., LTD.

City/State/Country

Shenzhen Guangdong, CN

Establishment Address

905, Bldg 1, Xinyi Lingyu R&D Center No.30, Honglang Beier Rd, Zone 69, Xingdong Community, Xin 'an Sub-district, Bao'an Dist, Shenzhen Guangdong 518000, CN

Establishment Type(s)

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

Owner / Operator

Shenzhen Xingyi Intelligent Technology Co., Ltd. (Owner Number: 10095015)

Owner / Operator Contact Address

905, Bldg 1, Xinyi Lingyu R&D Center No.30, Honglang Beier Rd, Zone 69, Xingdong Community, Xin 'an Sub-district, Bao'an Dist, Shenzhen, CN-GD 518000, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Mentra LIVE

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HQZ	Frame, Spectacle	Ophthalmic	Class 1	886.5842	2026-01-15

Official Correspondent

Vanda Geek

US Agent Details

Alexander Israelov Business: Mentra Labs Inc Email: tech@mentraglass.com Phone: (847) 7367492

Related Public Records

Same Entity

Shenzhen Xingyi Intelligent Technology 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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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3043656118. Last updated year: 2026. Please use registration number 3043656118 when referencing this establishment in official correspondence.