GUANGZHOU AIMEI INTELLIGENT TECHNOLOGY CO., LTD.

FDA Device Registration & Listing · Guangzhou Guangdong, CN · Registration 3030019171

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
3030019171
FEI Number
3030019171
Entity Name
GUANGZHOU AIMEI INTELLIGENT TECHNOLOGY CO., LTD.
City/State/Country
Guangzhou Guangdong, CN
Establishment Address
Floor 2 building B No.185, Zhongsheng Road, Zhongcun Street, Panyu District, Guangzhou Guangdong 511495, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Guangzhou Aimei Intelligent Technology Co., Ltd. (Owner Number: 10088981)
Owner / Operator Contact Address
Floor 2 building B No.185, Zhongsheng Road, Zhongcun Street, Panyu District, Guangzhou, CN-GD 511495, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Surgical Clipper;Model:LP001;LP003;Medical Clipper;Model:LP001;LP003 Nasal Aspirator DQ08,DQ18,DQ20,DQ22,DQ28,DQ30,DQ33,DQ38,DQ50,DQ58,DQ66,DQ68,DQ88,XD01,XD02,XD03,XD05,XD06,XD08,XD10,XD11 Surgical Clipper Blade;Model:LP002;LP004;Disposable surgical clipper blade;Model:LP002;LP004

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
JOK Scissors, Medical, Disposable General Hospital Class 1 880.6820 2026-05-26
KDQ Bottle, Collection, Vacuum General Hospital Class 2 880.6740 2023-10-25
GES Blade, Scalpel General, Plastic Surgery Class 1 878.4800 2026-05-26

Official Correspondent

No official correspondent registered.

US Agent Details

mark Yao Email: markFDA@outlook.com Phone: (303) 3594188

Related Public Records

Same Entity

Guangzhou Aimei Intelligent 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-0012-2008 Becton Dickinson & Company 1
Shelf Pack: Bard-Parker Rib-Back Carbon Steel no.11, surgical blade. Unit Package: Contents of unopened or undamaged package guaranteed sterile; After use place product in a puncture resistant container and dispose properly. Becton Dickinson Becton Dickinson Acute Care Franklin Lakes, NJ 07417
Z-0013-2008 Becton Dickinson & Company 1
Shelf Pack: Bard-Parker Rib-Back Stainless Steel no.11, surgical blade. Unit Package: Contents of unopened or undamaged package guaranteed sterile; After use place product in a puncture resistant container and dispose properly. Becton Dickinson Becton Dickinson Acute Care Franklin Lakes, NJ 07417

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3030019171. Last updated year: 2026. Please use registration number 3030019171 when referencing this establishment in official correspondence.
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