Data / Medical devices / South Korea / Ids Ltd
Ids Ltd: FDA-registered device maker in Geumcheon-gu Seoul, South Korea, 4 510(k) clearances
Ids Ltd is registered with the FDA (registration 3034246188) in Geumcheon-gu Seoul, South Korea. It lists 2 device types. The FDA files 4 510(k) clearances under its listings, the newest dated December 21, 2023. 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
- 3034246188
- Address
- RM.914, 915, SJ Techno Ville, 278, Beotkkot-ro, Geumcheon-gu, Seoul, 08511, KOREA, Geumcheon-gu Seoul, South Korea, 08511
- Owner or operator
- IDS LTD (10053355)
- Roles
- Manufacturer
- First device listed
- February 21, 2018
- Registered through
- 2026
- Brand names listed
- FRACLIGHT RPL System, PICO PREMIUM Picosecond Nd:YAG Laser System, Q10 Q-Switched Nd:YAG Laser System, REMOVER Alexandrite & Long Pulsed Nd:YAG Laser, SHINY PLUS, SHINY RPL System, SMARTRION COMBI Alexandrite & Long Pulsed Nd:YAG Laser, SOLALUX ALEX Alexandrite Laser and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Powered Laser Surgical Instrument | GEX | 2 | Manufacturer | accessdata.fda.gov |
| Powered Light Based Non-Laser Surgical Instrument With Thermal Effect | ONF | 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 21, 2023 | K233018 | PICOSECOND Nd:YAG Laser System | GEX | Substantially Equivalent | Ids, Ltd. | accessdata.fda.gov |
| March 29, 2023 | K222485 | SMARTRION COMBI/Alexandrite & Long Pulsed Nd:YAG Laser | GEX | Substantially Equivalent | Ids, Limited | accessdata.fda.gov |
| October 5, 2018 | K181868 | SHINY RPL System | ONF | Substantially Equivalent | Ids, Ltd. | accessdata.fda.gov |
| August 1, 2017 | K171079 | Q-Switched Nd:YAG Laser System | GEX | Substantially Equivalent | Ids, Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Powered Light Based Non-Laser Surgical Instrument With Thermal Effect
- All makers of Powered Laser Surgical Instrument
Updated December 21, 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.