Data / Medical devices / South Korea / Lhbiomed Co., Ltd.
Lhbiomed Co., Ltd.: FDA-registered device maker in Wonju-si Gangwon, South Korea, 1 510(k) clearance
Lhbiomed Co., Ltd. is registered with the FDA (registration 3038613815) in Wonju-si Gangwon, South Korea. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated August 7, 2024. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3038613815
- Address
- #806, Medical device Complex Center, 200, Gieopdosi-ro, Jijeong-myeon, Wonju-si Gangwon, South Korea, 26354
- Owner or operator
- LHbiomed Co., Ltd. (10093524)
- Roles
- Manufacturer
- First device listed
- May 28, 2025
- Registered through
- 2026
- Brand names listed
- EMULSIFY, LIPOSAVER
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| System, Suction, Lipoplasty For Removal | QPB | 2 | 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 |
|---|---|---|---|---|---|---|
| August 7, 2024 | K212969 | Liposaver | QPB | Substantially Equivalent | Lhbiomed Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated August 7, 2024. 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.