Light Tree Ventures Europe B.V.
Light Tree Ventures Europe B.V. holds FDA 510(k) medical device clearances, first cleared 2022, most recent 2026.
Top product codes for Light Tree Ventures Europe B.V.
Recent clearances by Light Tree Ventures Europe B.V.
- K260415 — myLEDmask 2 (MJ-144)
- K253349 — Hair Regrowth Cap (Model: T-119-HRC)
- K230720 — LUSTRE 3XPRESS Light Beauty Therapy patches, model: PR6001, PR5001
- K223893 — Infrared Heat (Model: E0221)
- K230042 — Q-Rejuvalight Pro Facewear (Model: P19-0023)
- K230597 — Aduro Comb (Model: SZ-22, SZ-22A, SZ-22B)
- K230336 — CurrentBody Skin Led Hair Regrowth(Model: MZ-07)
- K230124 — LUSTRE ClearSkin Renew Pro Facewear Mask(Model: PR4001)
- K223642 — LED Lip Perfector, model: ZC-05
- K221775 — LED Light Therapy Mask (model: MK-78, MK-04, MK66-H, MK66R-B, EL00003)
- K221444 — LED Eye Perfector, model: EY-36A, EY-36B
- K221946 — LED Light Therapy Mask (model: MK66R-B)
- K222205 — Cold Sore Device (Model: QPZ-01)
Data sourced from openFDA. This site is unofficial and independent of the FDA.