Data / Medical devices / South Korea / Medpark Co., Ltd.
Medpark Co., Ltd.: FDA-registered device maker in Busan, South Korea, 2 510(k) clearances
Medpark Co., Ltd. is registered with the FDA (registration 3029731364) in Busan, South Korea. It lists 2 device types. The FDA files 2 510(k) clearances under its listings, the newest dated June 16, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3029731364
- Address
- 24, nakdong-daero 1570beon-gil, buk-gu, busan, republic of korea, Busan, South Korea, 46504
- Owner or operator
- MEDPARK.Co., Ltd. (10088661)
- Roles
- Manufacturer
- First device listed
- October 1, 2023
- Registered through
- 2026
- Brand names listed
- Endobon® Bovine Xenograft Moldable, Endobon® Bovine Xenograft Particulate
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Bone Grafting Material, Animal Source | NPM | 2 | Manufacturer | accessdata.fda.gov |
| Orthopedic Manual Surgical Instrument | LXH | 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 |
|---|---|---|---|---|---|---|
| June 16, 2026 | K253723 | BOSS | NPM | Substantially Equivalent | Medpark Co., Ltd. | accessdata.fda.gov |
| October 13, 2023 | K231672 | S1 | NPM | Substantially Equivalent | Medpark Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Orthopedic Manual Surgical Instrument
- All makers of Bone Grafting Material, Animal Source
Updated June 16, 2026. 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.