PIGEON MANUFACTURING (SHANGHAI) CO.,LTD

FDA Device Registration & Listing · Shanghai, CN · Registration 3010531400

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
3010531400
FEI Number
3010531400
Entity Name
PIGEON MANUFACTURING (SHANGHAI) CO.,LTD
City/State/Country
Shanghai, CN
Establishment Address
No.405,Beiying Road, Qingpu Industrial Zone, Shanghai 201700, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
PIGEON SHANGHAI CO LTD (Owner Number: 10048391)
Owner / Operator Contact Address
Rm 3201-3203, 2 Grand Gateway, 3 Hongqiao Road,, Shanghai, CN-SH 200030, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Pigeon

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FNN Nipple, Lambs Feeding General Hospital Class 1 880.5640 2015-01-08

Official Correspondent

Mike Chen

US Agent Details

Jake He Business: Pigeon America Inc Email: Jake@us.pigeon.com Phone: (703) 2606970

Related Public Records

Same Entity

PIGEON SHANGHAI 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 3010531400. Last updated year: 2026. Please use registration number 3010531400 when referencing this establishment in official correspondence.
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