Fotona D.O.O.
Fotona D.O.O. holds FDA 510(k) medical device clearances, first cleared 2017, most recent 2025.
Top product codes for Fotona D.O.O.
Recent clearances by Fotona D.O.O.
- K241785 — StarFormer (M008-3T)
- K242202 — LightWalker Laser System Family
- K234061 — StarFormer
- K221274 — StarFormer, TightWave
- K223540 — AvalancheLase Family
- K221712 — Fotona XPulse Laser System Family (XPulse 1064 nm, XPulse 810 nm, XPulse 980 nm)
- K213267 — Dynamis Pro Family
- K202991 — Fotona XPulse Pro Laser Platform
- K202985 — LightWalker Laser System Family
- K202172 — StarWalker
- K193656 — SkyPulse
- K193661 — LightWalker Laser System Family
- K191554 — LightWalker Laser System Family
- K182088 — XS Dynamis, XP Dynamis, SP Dynamis, XP Spectro, SP Spectro
- K172819 — LightWalker Laser System Family
- K171227 — StarWalker
Data sourced from openFDA. This site is unofficial and independent of the FDA.