Data / Medical devices / South Korea / SRMC Co., Ltd.
SRMC Co., Ltd.: FDA-registered device maker in Cheongju-si Chungbuk, South Korea, 1 510(k) clearance
SRMC Co., Ltd. is registered with the FDA (registration 3033524191) in Cheongju-si Chungbuk, South Korea. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated December 24, 2014. 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
- 3033524191
- Address
- 7F, 1130, 2sunhwan-ro, Heungdeok-gu, Cheongju-si Chungbuk, South Korea, 28363
- Owner or operator
- SRMC CO., LTD. (10091883)
- Roles
- Manufacturer
- First device listed
- November 11, 2024
- Registered through
- 2026
- Brand names listed
- MiDi-SRS, SRA, SRR
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Massager, Therapeutic, Electric | ISA | 1 | Manufacturer | accessdata.fda.gov |
| Powered Laser Surgical Instrument | GEX | 2 | Manufacturer | accessdata.fda.gov |
| Powered Laser Surgical Instrument With MicrobeamFractional Output | ONG | 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 |
|---|---|---|---|---|---|---|
| December 24, 2014 | K141046 | MIDI-SRS | ONG | Substantially Equivalent | Srmc Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Powered Laser Surgical Instrument With MicrobeamFractional Output
- All makers of Powered Laser Surgical Instrument
- All makers of Massager, Therapeutic, Electric
Updated December 24, 2014. 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.