Zhejiang Tiansong Medical Instrument Co., Ltd

FDA Device Registration & Listing · Hangzhou Zhejiang, CN · Registration 3007710604

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
3007710604
FEI Number
3007710604
Entity Name
Zhejiang Tiansong Medical Instrument Co., Ltd
City/State/Country
Hangzhou Zhejiang, CN
Establishment Address
No.168, Jianduan Road, E&T Developing Zone, Hangzhou Zhejiang 311501, CN
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device
Owner / Operator
Zhejiang Tiansong Medical Instrument Co., Ltd (Owner Number: 10029837)
Owner / Operator Contact Address
No.168, Jianduan Road, E&T Developing Zone, Hangzhou, CN-ZJ 311501, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Grasping forceps:diameter:¢5/10mm Cystoscope:0° 30° 70° Scissors: diameter: ¢5/10mm,straight,curved,hooked Tissue dissecting forceps: diameter: ¢5/10mm

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HTD Forceps General, Plastic Surgery Class 1 878.4800 2009-07-01
FAJ Cystoscope And Accessories, Flexible/Rigid Gastroenterology, Urology Class 2 876.1500 2009-07-01
LRW Scissors, General, Surgical General, Plastic Surgery Class 1 878.4800 2009-07-01
GEN Forceps, General & Plastic Surgery General, Plastic Surgery Class 1 878.4800 2009-07-01

Official Correspondent

No official correspondent registered.

US Agent Details

Charles Mack Business: IRC USA Email: ircfda@gmail.com Phone: (931) 6254938

Related Public Records

Same Entity

Zhejiang Tiansong Medical Instrument Co., Ltd
View consolidated registration, premarket clearance, and recall records for this applicant.
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Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K852723 The Huxley Instrument Corp. FOERSTER SPONGE FORCEPS, SERRATED, 7+SS 410 OR 420 1985-07-15
K873512 Arthropedics, Inc. SERRATED GRASPING FORCEPS, RIGHT 1987-11-02
K851170 The Huxley Instrument Corp. DISSECTING TWEEZER #283-72PCS. SS 410 1985-04-25
K821248 Conphar, Inc. ROCHESTER PEAN FORCEPS 1982-05-28

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007710604. Last updated year: 2026. Please use registration number 3007710604 when referencing this establishment in official correspondence.
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