JIANGSU YONGLE MEDICAL TECHNOLOGY CO., LTD.

FDA Device Registration & Listing · Taixing City Jiangsu, CN · Registration 3017166758

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
3017166758
FEI Number
3017166758
Entity Name
JIANGSU YONGLE MEDICAL TECHNOLOGY CO., LTD.
City/State/Country
Taixing City Jiangsu, CN
Establishment Address
No.1, Jiaodang Industrial Cluster, Zhangqiao Town,, Taixing City Jiangsu 225400, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Jiangsu Yongle Medical Technology Co., Ltd. (Owner Number: 10049351)
Owner / Operator Contact Address
No.1, Jiaodang Industrial Cluster, Zhangqiao Town,, Taixing City, CN-JS 225400, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Laryngoscope Ent Manual Surgical Respirator

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
CCW Laryngoscope, Rigid Anesthesiology Class 1 868.5540 2015-05-15
LRC Instrument, Ent Manual Surgical Ear, Nose, Throat Class 1 874.4420 2023-06-07
MSH Respirator, Surgical General, Plastic Surgery Class 2 878.4040 2020-04-19

Official Correspondent

Daniel Ding

US Agent Details

Yu Ying Yi Email: hyy_01@hotmail.com Phone: (858) 7176557

Related Public Records

Same Entity

Jiangsu Yongle Medical Technology Co., 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
K143738 Intuit Medical Products, LLC DSS Sinusplasty Balloon Catheter 2015-08-27
K102092 Prestige Ameritech PRO GEAR N95 PARTICULATE FILTER RESPIRATOR & SURGICAL MASK, REGULAR SIZE MODEL RP CERIES 2010-10-06

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0144-2024 Covidien 1
Stolen McGRATH MAC Video Laryngoscopes, REF: 301-000-000
Z-0168-2024 Covidien 1
McGrath Mac 2, Disposable Laryngoscope Blade, REF: 350-017-000, Sterile EO, Rx Only
Z-0169-2024 Covidien 1
McGrath Mac 2, Disposable Laryngoscope Blade, REF: 350-084-000, Sterile EO, Rx Only

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3017166758. Last updated year: 2026. Please use registration number 3017166758 when referencing this establishment in official correspondence.
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