SUQIAN ZHENGTONG MEDICAL INSTRUMENTS CO. LTD

FDA Device Registration & Listing · CHINA, HK · Registration 3008342610

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
3008342610
FEI Number
3008342610
Entity Name
SUQIAN ZHENGTONG MEDICAL INSTRUMENTS CO. LTD
City/State/Country
CHINA, HK
Establishment Address
FACTORY: NO 6 TIANSHAN ROAD ECONOMIC, DEVELOPMENT ZONE SIHONG JIANGSU, CHINA 00000, HK
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device
Owner / Operator
NETWORK TECHNOLOGY DEVELOPMENT LTD (Owner Number: 10031992)
Owner / Operator Contact Address
61-63 Aupuiwan Street Yale Industrial Center Floor 10 Room 21, FOTAN, HONG KONG, HK-NOTA 00000, HK
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Network Technology Development Ltd Network Technology Development Ltd Network Technology Development Ltd network technology development ltd focus care Network Technology development ltd Network Technology Development Ltd focus FOCUS focus focus network technology development ltd focus Network Technology Development Ltd Network Technology Development Ltd Network Technology Development Ltd focus focus Network Technology Development Ltd Network Technology Development Ltd

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HRH Trephine, Manual, Ophthalmic Ophthalmic Class 1 886.4350 2018-01-16
HNB Spoon, Ophthalmic Ophthalmic Class 1 886.4350 2018-01-16
HMZ Trabeculotome Ophthalmic Class 1 886.4350 2018-01-16
HNC Specula, Ophthalmic Ophthalmic Class 1 886.4350 2018-01-16
HLF Device, Measuring, Lens Radius, Ophthalmic Ophthalmic Class 1 886.1430 2018-01-16
LYU Accessory, Surgical Apparel General, Plastic Surgery Class 1 878.4040 2020-05-26
HNJ Punch, Corneo-Scleral Ophthalmic Class 1 886.4350 2018-01-16
HNG Rongeur, Lachrymal Sac Ophthalmic Class 1 886.4350 2018-01-16
FHQ Holder, Needle, Gastroenterologic Gastroenterology, Urology Class 1 876.4730 2018-04-19
HNN Knife, Ophthalmic Ophthalmic Class 1 886.4350 2025-05-15
HMX Cannula, Ophthalmic Ophthalmic Class 1 886.4350 2011-01-11
HND Spatula, Ophthalmic Ophthalmic Class 1 886.4350 2011-01-11
HNL Probe, Lachrymal Ophthalmic Class 1 886.4350 2018-01-16
HOE Caliper, Ophthalmic Ophthalmic Class 1 886.4350 2011-01-11
HMQ Marker, Sclera Ophthalmic Class 1 886.4570 2018-01-16
HNH Ring, Ophthalmic (Flieringa) Ophthalmic Class 1 886.4350 2018-01-16
HNQ Hook, Ophthalmic Ophthalmic Class 1 886.4350 2010-05-20
HNX Depressor, Orbital Ophthalmic Class 1 886.4350 2018-01-16
HNI Retractor, Ophthalmic Ophthalmic Class 1 886.4350 2011-01-11
HND Spatula, Ophthalmic Ophthalmic Class 1 886.4350 2011-01-11
HNK Probe, Trabeculotomy Ophthalmic Class 1 886.4350 2018-01-16
HNW Dilator, Lachrymal Ophthalmic Class 1 886.4350 2018-01-16

Official Correspondent

ZHENG CHEN

US Agent Details

Lisa L Delorey DELOREY Email: awesomemom80@gmail.com Phone: (727) 7769627

Related Public Records

Same Entity

NETWORK TECHNOLOGY DEVELOPMENT LTD
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K871646 Ocular Instruments, Inc. TANNE CORNEAL CUTTING BLOCK 1987-05-18
K874057 Myocure, Inc. OPHTHALMIC TIP & BLADE SCALPELS 1987-12-23
K854401 Microsurgical Technology, Inc. THE NEW MOBILE TIP MCINTYRE CANNULA 1985-12-30

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0026-04 Surgical Specialties Corp 1
Sharpoint 2.75 mm x 3.75 mm ClearTrap Trapezoid Knife Clear Corneal Implant Angled. The product can be sold as an individual unit or in a box of 6 knives.
Z-1922-2024 Alcon Research LLC Aspex Facility 1
20 Gauge V-Lance Knife Model/Catalog Number: 8065912001 Software Version: N/A Product Description: Ophthalmic knife Component: N/A
Z-1923-2024 Alcon Research LLC Aspex Facility 1
ClearCut Sideport Knife Dual Bevel 1.2mm Angled Model/Catalog Number: 8065921541 Software Version: N/A Product Description: Ophthalmic Knife Component: N/A
Z-1924-2024 Alcon Research LLC Aspex Facility 1
ClearCut S Safety Sideport Knife 1.0mm Dual Bevel Model/Catalog Number: 8065771540 Software Version: N/A Product Description: Ophthalmic Knife Component: N/A
Z-1925-2024 Alcon Research LLC Aspex Facility 1
ClearCut S Safety Sideport Knife 1.2mm Dual Bevel Model/Catalog Number: 8065771541 Software Version: N/A Product Description: Ophthalmic Knife Component: N/A

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008342610. Last updated year: 2026. Please use registration number 3008342610 when referencing this establishment in official correspondence.
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