Data / Medical devices / Taiwan / Li Medical Corporation Ltd.
Li Medical Corporation Ltd.: FDA-registered device maker in New Taipei City, Taiwan, 4 510(k) clearances
Li Medical Corporation Ltd. is registered with the FDA (registration 3025325116) in New Taipei City, Taiwan. It lists 6 device types. The FDA files 4 510(k) clearances under its listings, the newest dated November 26, 2025. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3025325116
- Address
- 2F-4F., No. 58, Nanxing Rd., Xizhi Dist., New Taipei City, Taiwan, 221026
- Owner or operator
- LI MEDICAL CORPORATION LTD. (10086102)
- Roles
- Foreign private label distributor, Manufacturer
- First device listed
- October 16, 2022
- Registered through
- 2027
- Brand names listed
- "RELIEEV" Suction Curette (Flexible 3/ Standard 3.6), CERVICAL DILATOR, Pessary Remover, RELIEEV HSG Catheter (HSG7FA1), RELIEEV Vaginal Pessary, Uterine Sound, RELIEEV Uterine Manipulator Injector
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Cannula, Manipulator/Injector, Uterine | LKF | 2 | Foreign private label distributor, Manufacturer | accessdata.fda.gov |
| Curette, Suction, Endometrial (And Accessories) | HHK | 2 | Foreign private label distributor, Manufacturer | accessdata.fda.gov |
| Dilator, Cervical, Fixed Size | HDQ | 1 | Manufacturer | accessdata.fda.gov |
| Pessary, Vaginal | HHW | 2 | Foreign private label distributor, Manufacturer | accessdata.fda.gov |
| Remover, Intrauterine Device, Contraceptive, Hook-Type | HHF | 1 | Manufacturer | accessdata.fda.gov |
| Sound, Uterine | HHM | 1 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| November 26, 2025 | K252260 | RELIEEV HSG Catheter (HSG7FA1) | LKF | Substantially Equivalent | Li Medical Corporation , Ltd. | accessdata.fda.gov |
| October 16, 2024 | K240364 | RELIEEV Uterine Manipulator Injector (CUMI 5.0) | LKF | Substantially Equivalent | Li Medical Corporation , Ltd. | accessdata.fda.gov |
| September 25, 2024 | K240434 | RELIEEV Suction Curette (Flexible 3.0/ Standard 3.6) | HHK | Substantially Equivalent | Li Medical Corporation , Ltd. | accessdata.fda.gov |
| November 18, 2003 | K031463 | MARINA MEDICAL SILICONE PESSARY | HHW | Substantially Equivalent | Marina Medical Instruments, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Cannula, Manipulator/Injector, Uterine
- All makers of Sound, Uterine
- All makers of Curette, Suction, Endometrial (And Accessories)
- All makers of Dilator, Cervical, Fixed Size
- All makers of Pessary, Vaginal
- All makers of Remover, Intrauterine Device, Contraceptive, Hook-Type
Updated November 26, 2025. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.