Data / Medical devices / South Korea / Unilam Co., Ltd.
Unilam Co., Ltd.: FDA-registered device maker in Ulju-Gun Ulsan, South Korea, 1 510(k) clearance
Unilam Co., Ltd. is registered with the FDA (registration 3007123863) in Ulju-Gun Ulsan, South Korea. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated February 15, 2023. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3007123863
- Address
- 23 Samdong-Ro, Samnam-Myeon, Ulju-Gun, Ulju-Gun Ulsan, South Korea, 44954
- Owner or operator
- Unilam Co., Ltd (10026373)
- Roles
- Manufacturer
- First device listed
- October 12, 2023
- Registered through
- 2026
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Booth, Sun Tan | LEJ | 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 |
|---|---|---|---|---|---|---|
| February 15, 2023 | K221523 | Tanning Lamp | LEJ | Substantially Equivalent | Unilam Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated February 15, 2023. 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.