Light Tree Ventures Europe B.V. - FDA 510(k) Cleared Devices
12
Total
12
Cleared
0
Denied
Light Tree Ventures Europe B.V. has 12 FDA 510(k) cleared general & plastic surgery devices. Based in Den Haag, NL.
Latest FDA clearance: Dec 2025. Active since 2022.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Shenzhen Kaiyan Medical Equipment Co., Ltd. as regulatory consultant.
12 devices
Cleared
Dec 24, 2025
Hair Regrowth Cap (Model: T-119-HRC)
General & Plastic Surgery
85d
Cleared
Jul 03, 2023
LUSTRE 3XPRESS Light Beauty Therapy patches, model: PR6001, PR5001
General & Plastic Surgery
109d
Cleared
May 16, 2023
Infrared Heat (Model: E0221)
General & Plastic Surgery
139d
Cleared
Apr 28, 2023
Q-Rejuvalight Pro Facewear (Model: P19-0023)
General & Plastic Surgery
112d
Cleared
Apr 28, 2023
Aduro Comb (Model: SZ-22, SZ-22A, SZ-22B)
General & Plastic Surgery
56d
Cleared
Apr 05, 2023
CurrentBody Skin™ Led Hair Regrowth(Model: MZ-07)
General & Plastic Surgery
57d
Cleared
Mar 15, 2023
LUSTRE ClearSkin Renew Pro Facewear Mask(Model: PR4001)
General & Plastic Surgery
57d
Cleared
Mar 09, 2023
LED Lip Perfector, model: ZC-05
General & Plastic Surgery
93d
Cleared
Dec 20, 2022
LED Light Therapy Mask (model: MK-78, MK-04, MK66-H, MK66R-B, EL00003)
General & Plastic Surgery
182d
Cleared
Dec 08, 2022
LED Eye Perfector, model: EY-36A, EY-36B
General & Plastic Surgery
204d
Cleared
Nov 22, 2022
LED Light Therapy Mask (model: MK66R-B)
General & Plastic Surgery
140d
Cleared
Oct 07, 2022
Cold Sore Device (Model: QPZ-01)
General & Plastic Surgery
74d