LI MEDICAL CORPORATION LTD.

FDA Device Registration & Listing · New Taipei City, TW · Registration 3025325116

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
3025325116
FEI Number
3025325116
Entity Name
LI MEDICAL CORPORATION LTD.
City/State/Country
New Taipei City, TW
Establishment Address
2F-4F., No. 58, Nanxing Rd., Xizhi Dist., New Taipei City 221026, TW
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
LI MEDICAL CORPORATION LTD. (Owner Number: 10086102)
Owner / Operator Contact Address
2F., No. 43, Zhongxing Rd., Xizhi Dist.,, New Taipei City, TW-NOTA 221012, TW
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

CERVICAL DILATOR “RELIEEV” Uterine Manipulator Injector RELIEEV Vaginal Pessary RELIEEV HSG Catheter (HSG7FA1) "RELIEEV" Suction Curette (Flexible 3/ Standard 3.6) Pessary Remover

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HDQ Dilator, Cervical, Fixed Size Obstetrics/Gynecology Class 1 884.4530 2022-10-16
LKF Cannula, Manipulator/Injector, Uterine Obstetrics/Gynecology Class 2 884.4530 2024-12-04
HHW Pessary, Vaginal Obstetrics/Gynecology Class 2 884.3575 2025-02-15
LKF Cannula, Manipulator/Injector, Uterine Obstetrics/Gynecology Class 2 884.4530 2025-12-10
HHK Curette, Suction, Endometrial (And Accessories) Obstetrics/Gynecology Class 2 884.1175 2024-12-04
HHF Remover, Intrauterine Device, Contraceptive, Hook-Type Obstetrics/Gynecology Class 1 884.4530 2022-10-16

Official Correspondent

Eric Pan

US Agent Details

King Liang Email: kingster4life@yahoo.com Phone: (408) 2308215

Related Public Records

Same Entity

LI MEDICAL CORPORATION 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
K933654 Johnson & Johnson Medical, Inc. BLADDER NECK SUPPORT PROTHESIS FITTING KIT 1995-05-04

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3025325116. Last updated year: 2026. Please use registration number 3025325116 when referencing this establishment in official correspondence.
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