WELL CARE (WUHAN) MEDICAL TECHNOLOGY CO., LTD.

FDA Device Registration & Listing · Wuhan Hubei, CN · Registration 3022555975

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
3022555975
FEI Number
3022555975
Entity Name
WELL CARE (WUHAN) MEDICAL TECHNOLOGY CO., LTD.
City/State/Country
Wuhan Hubei, CN
Establishment Address
No. 11# The No.1 road Fozuling of East Lake High-Tech Development Zone, Wuhan Hubei 430205, CN
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device
Owner / Operator
Well care (Wuhan) medical technology Co., Ltd. (Owner Number: 10084681)
Owner / Operator Contact Address
No. 11# The No.1 road Fozuling of East Lake High-Tech Development Zone, Wuhan, CN-HB 430205, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Quantitative Tighten Elastic Thread Ligator for Hemorrhoids Automatic Tightening Band Ligation for Hemorrhoids Speculum, Rectal WellCare Anoscope

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FHN Ligator, Hemorrhoidal Gastroenterology, Urology Class 2 876.4400 2022-03-21
FFQ Speculum, Rectal Gastroenterology, Urology Class 1 876.4730 2025-12-17
FER Anoscope And Accessories Gastroenterology, Urology Class 2 876.1500 2024-01-03

Official Correspondent

Huimin Zhou

US Agent Details

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

Related Public Records

Same Entity

Well care (Wuhan) 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
K000397 Boston Scientific Corp SPEEDBAND SUPERVIEW MULTIPLE BAND LIGATOR, MODELS 4225, 4228; INJECTION SPEEDBAND SUPERVIEW MULTIPLE BAND LIGATOR, MODEL 2000-03-07

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3022555975. Last updated year: 2026. Please use registration number 3022555975 when referencing this establishment in official correspondence.
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