Laseroptek
Active in EUDAMEDSouth Koreafrom SRN EUDAMED FDA SRN KR-MF-000018426 FEI 3007181527
- Devices
- 6
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
At a glance
Market reach
- European Union
- EUDAMED actor
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Regimes: CE MDD Registry: EUDAMED
- Regimes: CE MDD Registry: EUDAMED
- Regimes: CE MDD Registry: EUDAMED
- Regimes: CE MDD Registry: EUDAMED
- Regimes: CE MDD Registry: EUDAMED
- Regimes: CE MDD Registry: EUDAMED
Company details
- EUDAMED SRN
- KR-MF-000018426
- FDA FEI number
- 3007181527
- EUDAMED status
- Active
- EUDAMED registered name
- Laseroptek
- Registered address
- 31, Galmachi-ro 244beon-gil, Jungwon-gu,, 13212, Seongnam-si, Gyeonggi-do, South Korea
- [email protected]
- PRRC contact
- Kyeong Tae KIM
Frequently asked questions
How many devices does Laseroptek have in the registry?
The registry currently lists 6 devices for Laseroptek. Devices recorded under merged duplicate company entries are counted once.
Which registries list Laseroptek's devices?
Among its 6 most recently registered devices, Laseroptek has devices listed in EUDAMED (6 devices).
What risk classes do Laseroptek's devices fall under?
Among its 6 most recently registered devices, the classes recorded for Laseroptek's devices are Class IIb. Each device page shows its own class and authorisation.
What are the newest devices from Laseroptek in the registry?
The most recently registered devices listed for Laseroptek include HELIOS 785 Pico, PALLAS, LOTUS III and PicoLO PREMIUM.