Data / Medical devices / South Korea / VIOL Medical CO., LTD.
VIOL Medical CO., LTD.: FDA-registered device maker in Seongnam-si Gyeonggi, South Korea, 5 510(k) clearances
VIOL Medical CO., LTD. is registered with the FDA (registration 3009206941) in Seongnam-si Gyeonggi, South Korea. It lists 1 device type. The FDA files 5 510(k) clearances under its listings, the newest dated August 27, 2026. Registered through 2026. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 3009206941
- Address
- C-209-1, 802~809, Bundang Technopark C 744, Pangyo-ro, Bundang-gu, Seongnam-si Gyeonggi, South Korea, 13510
- Owner or operator
- VIOL Medical Co., Ltd. (10056117)
- Roles
- Manufacturer
- First device listed
- November 7, 2017
- Registered through
- 2026
- Brand names listed
- CELFIRM, CELLINEW, SCARLET PRO, SCARLET S, SYLFIRM, SYLFIRM X
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Electrosurgical, Cutting & Coagulation & Accessories | GEI | 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 27, 2026 | K253859 | Scarlet Pro (Scarlet Pro) | GEI | Substantially Equivalent | VIOL Co., Ltd. | accessdata.fda.gov |
| November 26, 2024 | K240897 | Cellinew | GEI | Substantially Equivalent | VIOL Co., Ltd. | accessdata.fda.gov |
| June 23, 2022 | K213612 | SYLFIRM X | GEI | Substantially Equivalent | VIOL Co., Ltd. | accessdata.fda.gov |
| October 11, 2018 | K180872 | SCARLET SRF | GEI | Substantially Equivalent | VIOL Co., Ltd. | accessdata.fda.gov |
| October 13, 2017 | K172023 | CELFIRM | GEI | Substantially Equivalent | VIOL Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated August 27, 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.