Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3042262503

FEI Number

3042262503

Entity Name

CHENGDU TINGFENG BIOTECHNOLOGY CO., LTD.

City/State/Country

Chengdu Sichuan, CN

Establishment Address

No. 5 Building, No. 1919 Shuangyan Road, Chengdu Strait Cross-Strait Science and Technology Industry Development Zone, Wenjiang District, Chengdu Sichuan 611100, CN

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Chengdu Tingfeng Biotechnology Co., Ltd. (Owner Number: 10094245)

Owner / Operator Contact Address

Building 2, international financial center, No.1, section 3, Hongxing Road, Jinjiang District, Chengdu, CN-SC 610041, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

HealCheck Pee Cup

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NNI	Container, Specimen, Non-Sterile	Pathology	Class 1	864.3250	2025-11-20

Official Correspondent

Suting Duan

US Agent Details

Bryan Fang Email: ella.yuan@healgen.com Phone: (866) 9823818

Related Public Records

Same Entity

Chengdu Tingfeng Biotechnology Co., Ltd.

View consolidated registration, premarket clearance, and recall records for this applicant.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3042262503. Last updated year: 2026. Please use registration number 3042262503 when referencing this establishment in official correspondence.