CORITON INSTRUMENT CO., LTD.

FDA Device Registration & Listing · Shenzhen Guangdong, CN · Registration 3013182765

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
3013182765
FEI Number
3013182765
Entity Name
CORITON INSTRUMENT CO., LTD.
City/State/Country
Shenzhen Guangdong, CN
Establishment Address
5F Building C, Gold Power Industry Park, Julongshan Grand Industrial Zone, Pingshan Dist.,, Shenzhen Guangdong 518118, CN
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer),Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device
Owner / Operator
CORITON INSTRUMENT CO., LTD. (Owner Number: 10053185)
Owner / Operator Contact Address
5F Building C, Gold Power Industry Park, Julongshang Grand Industrial Zone, Pingshan Dist.,, Shenzhen, CN-GD 518118, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Pivot Arm,Variable Height Mount Fixed and Variable Height Roll Cart, Roll Stand Endoscopy Cart Patient Monitor Wall Mount, Wall Mount, Display Mount, Ventilator Arm, ECG Arm Ultrasound Cart, Medical Cart, Nursing card, Display Cart, Equipment Cart Patient Monitor Roll Stand, INFUSION Roll Stand, ECG Trolley, Pad Roll Stand, Medical Trolley, Display Trolley Computer Cart

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FOX Stand, Infusion General Hospital Class 1 880.6990 2016-11-07

Official Correspondent

Golden Guo

US Agent Details

WINNIE Zhu Business: Umedwings Solution USA Email: Agent@Umedwings.Us Phone: (224) 4023150

Related Public Records

Same Entity

CORITON INSTRUMENT CO., LTD.
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013182765. Last updated year: 2026. Please use registration number 3013182765 when referencing this establishment in official correspondence.
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