CHENGDU WISION MEDICAL DEVICE CO., LTD.

FDA Device Registration & Listing · Chengdu Sichuan, CN · Registration 3016591389

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3016591389
FEI Number
3016591389
Entity Name
CHENGDU WISION MEDICAL DEVICE CO., LTD.
City/State/Country
Chengdu Sichuan, CN
Establishment Address
Unit 802, Floor 8, Building 17, Yintaicheng, No.1999 Yizhou Road, Wuhou District, Chengdu Sichuan 610041, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Chengdu Wision Medical Device Co., Ltd. (Owner Number: 10084846)
Owner / Operator Contact Address
Unit 802, Floor 8, Building 17, Yintaicheng, No.1999 Yizhou Road, Wuhou District, Chengdu, CN-SC 610041, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K211326
PMA Number
N/A

All Registered Proprietary Names

EndoScreener

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
QNP Gastrointesinal Lesion Software Detection System Gastroenterology, Urology Class 2 876.1520 2022-04-06

Official Correspondent

Jiong He

US Agent Details

Xiao Xiao Email: support@wision.com Phone: (857) 2689686

Related Public Records

Same Entity

Chengdu Wision Medical Device Co., Ltd.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Similar Registrations

Registration Number Establishment Name Location
8010047 OLYMPUS MEDICAL SYSTEMS CORP. HACHIOJI-SHI Tokyo, JP
9610877 HOYA Corporation PENTAX Lifecare Division Akishima-shi Tokyo, JP
3018899987 COSMO ARTIFICIAL INTELLIGENCE, LTD Dublin 2, IE
3030626336 MAGENTIQ EYE LTD Haifa, IL
3016432796 MB Elettronica S.r.l. Cortona Arezzo, IT
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3016591389. Last updated year: 2026. Please use registration number 3016591389 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.