Laseroptek Co., Ltd.
Laseroptek Co., Ltd. holds FDA 510(k) medical device clearances, first cleared 2009, most recent 2025.
Top product codes for Laseroptek Co., Ltd.
Recent clearances by Laseroptek Co., Ltd.
- K243780 — HELIOS 785 Pico (1754V2)
- K230373 — HELIOS 785 Pico
- K223588 — PALLAS Premium
- K212663 — HELIOS IV 785
- K212573 — PicoLO Premium
- K203491 — PicoLO Nd: YAG Picosecond Laser System
- K191501 — PALLAS 308/311 Solid-State UV Laser System
- K183392 — PicoLO Nd:YAG Picosecond Laser System
- K182045 — Lotus III Multi-Pulsed Er: Yag Laser System
- K172639 — PALLAS 308/311 Solid-State UV Laser System
- K152856 — Helios III
- K083253 — LOTUS II PULSED ER: YAG LASER SYSTEM
- K083203 — HELIOS II Q-SWITCHED ND:YAG LASER SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.