Jeisys Medical, Inc. - FDA 510(k) Cleared Devices
15
Total
15
Cleared
0
Denied
Jeisys Medical, Inc. has 15 FDA 510(k) cleared general & plastic surgery devices. Based in Littleton, US.
Latest FDA clearance: Dec 2024. Active since 2008.
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.
FDA 510(k) cleared devices by Jeisys Medical, Inc.
15 devices
Cleared
Dec 10, 2024
POTENZA
General & Plastic Surgery
592d
Cleared
Nov 05, 2024
POTENZA
General & Plastic Surgery
551d
Cleared
Aug 14, 2023
Density
General & Plastic Surgery
157d
Cleared
Jan 04, 2023
SmoothCool HR System
General & Plastic Surgery
26d
Cleared
Apr 20, 2022
SmoothCool HR System
General & Plastic Surgery
173d
Cleared
Jan 19, 2021
Potenza
General & Plastic Surgery
211d
Cleared
Jan 15, 2020
INTRAcel RF Microneedle System
General & Plastic Surgery
415d
Cleared
Oct 18, 2019
LIPOcel
General & Plastic Surgery
459d
Cleared
Oct 27, 2016
EdgeOne CO2 Laser
General & Plastic Surgery
85d
Cleared
Jul 21, 2016
INTRAcel Premium Fractional RF Micro Needle (FRM) System
General & Plastic Surgery
206d
Cleared
Jun 04, 2015
INTRAGen
General & Plastic Surgery
247d
Cleared
Jan 07, 2015
HILTHERA 4.0
Physical Medicine
181d