Alma Lasers , Ltd.
Alma Lasers , Ltd. holds FDA 510(k) medical device clearances, first cleared 2007, most recent 2022.
Top product codes for Alma Lasers , Ltd.
Recent clearances by Alma Lasers , Ltd.
- K212073 — Alma Diode Tabletop Laser
- K203441 — The Alma Hybrid Laser System
- K170850 — Alma Q
- K140009 — SOPRANO ICE MULTI-APPLICATION & MULTI-TECHNOLOGY PLATFORM
- K140005 — ALMA DIODE TABLETOP LASER
- K090571 — ALMA LASERS ALEX755 MODULE
- K083848 — ALMA LASERS SOPRANO XL MULTI-APPLICATION PLATFORM
- K082622 — ALMA LASERS ACCENT B-SHAPE MASSAGER HANDPIECE/MODULE
- K080463 — ALMA LASERS THERMOXEL CO2 LASER SYSTEM AND DELIVERY DEVICE ACCESSORIES
- K072182 — ALMA LASERS FAMILY OF THERMO-XEL HANDPIECES, PIXEL MODELS: 2940, 1060
- K072564 — ALMA LASERS HARMONY XL MULTI-APPLICATION PLATFORM
- K080318 — ALMA LASER NIR MODULE
- K072699 — ALMA LASERS FAMILY OF ACCENT RADIOFREQUENCY (RF) SYSTEMS, MODELS: ACCENT, ACCENT XL
- K070004 — ACCENT
Data sourced from openFDA. This site is unofficial and independent of the FDA.