YUYAO GUANGJING MEDICAL INSTRUMENT CO.,LTD

FDA Device Registration & Listing · Ningbo Zhejiang, CN · Registration 3014313732

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
3014313732
FEI Number
3014313732
Entity Name
YUYAO GUANGJING MEDICAL INSTRUMENT CO.,LTD
City/State/Country
Ningbo Zhejiang, CN
Establishment Address
N0.126,HOU ZHONGCUN ROAD,MUHU VILLAGE,, DITANG STREET ,YUYAO,NINGBO, Ningbo Zhejiang 315400, CN
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device
Owner / Operator
YUYAO GUANGJING MEDICAL INSTRUMENT CO.,LTD (Owner Number: 10057023)
Owner / Operator Contact Address
N0.126,HOU ZHONGCUN ROAD,MUHU VILLAGE,, DITANG STREET ,YUYAO,NINGBO, Ningbo, CN-ZJ 315400, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Nasal speculum TOURNIQUET,PNEUMATIC BITE BLOCK SPORT TAPE TOURNIQUET, Buckle Tourniquet Nasal irrigator

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EPY Speculum, Ent General, Plastic Surgery Class 1 878.1800 2023-07-11
KCY Tourniquet, Pneumatic General, Plastic Surgery Class 1 878.5910 2021-12-19
MNK Endoscopic Bite Block Gastroenterology, Urology Class 1 876.1500 2018-02-12
KGX Tape And Bandage, Adhesive General Hospital Class 1 880.5240 2018-02-12
GAX Tourniquet, Nonpneumatic General, Plastic Surgery Class 1 878.5900 2018-02-12
KMA Irrigator, Powered Nasal Ear, Nose, Throat Class 1 874.5550 2023-07-11

Official Correspondent

HANXIONG Xu

US Agent Details

Leeyeo Kee Business: Regrek LLC Email: regrek.cs@hotmail.com Phone: (302) 6089028

Related Public Records

Same Entity

YUYAO GUANGJING MEDICAL INSTRUMENT 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
K834189 Imm Enterprises , Ltd. JAKOBI SURG. INSTRUMENTS #7 44/47 1984-03-06
K843874 Beiersdorf, Inc. LEUKOPOR SURGICAL TAPE 1985-02-21
K915446 Sun Glitz Corp. STRETCH WRAP 1992-05-06
K833120 Acme United Corp. ONE TIME COMPOUND BENZOIN TINCTURE- 1983-12-29
K870091 Avery Intl. IV SECUREMENT DEVICE USING PCCE THERMO. FILM 1987-02-04

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3003334541 CONCISE ENTERPRISES Sialkot Punjab, PK
3004892425 SPARTECH INSTRUMENTS & CO. SIALKOT, PUNJAB, PK
9680735 HERMANN MUELLER Medizintechnik GmbH TUTTLINGEN Baden-Wurttemberg, DE
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014313732. Last updated year: 2026. Please use registration number 3014313732 when referencing this establishment in official correspondence.
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