SUZHOU BENTENG SCIENCE & TECHNOLOGY CO., LTD

FDA Device Registration & Listing · Suzhou Jiangsu, CN · Registration 3013174542

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
3013174542
FEI Number
3013174542
Entity Name
SUZHOU BENTENG SCIENCE & TECHNOLOGY CO., LTD
City/State/Country
Suzhou Jiangsu, CN
Establishment Address
No. 57 Jinshang Road, Suzhou Industrial Park, Suzhou Area, China (Jiangsu) Pilot Free Trade, Suzhou Jiangsu 215123, CN
Establishment Type(s)
Manufacture Medical Device,Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Suzhou Benteng Science & Technology Co., Ltd (Owner Number: 10058223)
Owner / Operator Contact Address
No. 57 Jinshang Road, Suzhou Industrial Park,, Suzhou Area, China (Jiangsu) Pilot Free Trade, Suzhou, CN-JS 215123, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Foam Only Needle Nest, 9-Up Bullet, Foam Block with Cup Scalpel Holder, Red Syringe Cup, Red; Needle Nest, Cardinal Foam Block with Cup Needle Nest, Bard-Parker, Foam Block with Cup Needle Nest, Cardinal

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FSM Tray, Surgical, Instrument General, Plastic Surgery Class 1 878.4800 2018-08-01

Official Correspondent

No official correspondent registered.

US Agent Details

Jessie Yao Business: MEDRIGHT TECH INC Email: info@medright-tech.com Phone: (718) 2169957

Related Public Records

Same Entity

Suzhou Benteng Science & 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-0027-2016 Zimmer, Inc. 1
Zimmer Universal Locking System, Titanium 3.5mm. Zimmer Implant and Instrument Cases are reusable, non-implantable devices designed to facilitate organization, identification, storage, transportation, cleaning, and sterilization processing of reusable instruments and certain unused implantable devices.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013174542. Last updated year: 2026. Please use registration number 3013174542 when referencing this establishment in official correspondence.
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