Pollogen, Ltd. - FDA 510(k) Cleared Devices
18
Total
18
Cleared
0
Denied
Pollogen, Ltd. has 18 FDA 510(k) cleared general & plastic surgery devices. Based in Binyamina, IL.
Latest FDA clearance: Oct 2025. Active since 2011.
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.
Regulatory submissions have been managed by BioVision , Ltd., Regulatory Technology Services, LLC and The RC Insight Group, LLC.
18 devices
Cleared
Oct 12, 2025
GENEO X ELITE
General & Plastic Surgery
439d
Cleared
Sep 12, 2025
Legend X Platform
Neurology
29d
Cleared
Sep 10, 2025
OptiLUV Device
General & Plastic Surgery
183d
Cleared
Nov 01, 2024
Legend X Desktop System
General & Plastic Surgery
29d
Cleared
May 08, 2024
Legend X Applicator VO
General & Plastic Surgery
27d
Cleared
May 07, 2024
Geneo X Elite
General & Plastic Surgery
165d
Cleared
Oct 17, 2023
Legend X Platform
General & Plastic Surgery
29d
Cleared
May 04, 2023
Pollogen STOP U Model UXV Device
General & Plastic Surgery
455d
Cleared
Feb 17, 2022
YandR System, VoluDerm Handpiece, VoluDerm Tips
General & Plastic Surgery
30d
Cleared
Oct 21, 2021
Legend Pro DMA
Neurology
597d
Cleared
Feb 25, 2021
STOP U Model UXV Device
General & Plastic Surgery
71d
Cleared
Jun 19, 2019
STOP U (Packed Black USA), STOP U (Packed White USA)
General & Plastic Surgery
261d