TDG TECHNOLOGY CO., LTD.

FDA Device Registration & Listing · Jiaxing City Zhejiang, CN · Registration 3042254935

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
3042254935
FEI Number
3042254935
Entity Name
TDG TECHNOLOGY CO., LTD.
City/State/Country
Jiaxing City Zhejiang, CN
Establishment Address
No.1, Yatai Road, Nanhu District, Jiaxing City Zhejiang 314000, CN
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
TDG Technology Co., Ltd. (Owner Number: 10094163)
Owner / Operator Contact Address
No.1, Yatai Road, Nanhu District, Jiaxing City, CN-ZJ 314000, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Cuffill - Cuff Pressure Regulator

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
BSK Cuff, Tracheal Tube, Inflatable Anesthesiology Class 2 868.5750 2025-11-17

Official Correspondent

No official correspondent registered.

US Agent Details

Rosanna Lee Business: Simcon International LLC Email: rlee@simconintl.com Phone: (847) 9492290

Related Public Records

Same Entity

TDG Technology Co., Ltd.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0006-2014 H & H Associates 2
H&H Emergency Cricothyrotomy Kit (Part No. HHECT01/ HHECTK01, NSN 6515-01-573-0692), vacuum sealed and packaged in a 5 mil poly bags, labeled in part ***H & H Associates, Inc. CAGE 1NNH6 www.gohandh.com Ordinary, VA 23131 (800) 326-5708***. The product is used to maintain fracture alignment.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3042254935. Last updated year: 2026. Please use registration number 3042254935 when referencing this establishment in official correspondence.
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