NANJING TIANLANG PHARMACEUTICAL COMPANY LTD

FDA Device Registration & Listing · Nanjing City Jiangsu, CN · Registration 3035783442

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
3035783442
FEI Number
3035783442
Entity Name
NANJING TIANLANG PHARMACEUTICAL COMPANY LTD
City/State/Country
Nanjing City Jiangsu, CN
Establishment Address
No. 8 Shuibao Road, Yongyang Town, Lishui District, Nanjing City Jiangsu 210000, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Nanjing Tianlang Pharmaceutical Company Ltd (Owner Number: 10092332)
Owner / Operator Contact Address
No. 8 Shuibao Road, Yongyang Town, Lishui District, Nanjing City, CN-JS 210000, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
PFP Silicone Hydrogel For Scar Management General, Plastic Surgery Class 1 878.4025 2024-12-24

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

Nanjing Tianlang Pharmaceutical Company 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 3035783442. Last updated year: 2026. Please use registration number 3035783442 when referencing this establishment in official correspondence.
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