Cynosure, Inc. - FDA 510(k) Cleared Devices
98
Total
98
Cleared
0
Denied
Cynosure, Inc. has 98 FDA 510(k) cleared general & plastic surgery devices. Based in Bedford, US.
Historical record: 98 cleared submissions from 1992 to 2019.
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 Cynosure, Inc.
98 devices
Cleared
Jul 24, 2019
TempSure
General & Plastic Surgery
128d
Cleared
Oct 24, 2018
TempSure System
General & Plastic Surgery
55d
Cleared
Feb 07, 2018
PicoSure Workstation
General & Plastic Surgery
128d
Cleared
Sep 26, 2017
SculpSure
General & Plastic Surgery
85d
Cleared
Sep 22, 2017
TempSure
General & Plastic Surgery
144d
Cleared
Jun 13, 2017
Sculpsure
General & Plastic Surgery
60d
Cleared
Jul 21, 2016
SculpSure
General & Plastic Surgery
153d
Cleared
May 17, 2016
PicoSure Workstation
General & Plastic Surgery
85d
Cleared
Jul 01, 2015
SculpSure
General & Plastic Surgery
103d
Cleared
May 15, 2015
SculpSure
General & Plastic Surgery
102d
Cleared
Feb 23, 2015
Picosure Workstation
General & Plastic Surgery
117d
Cleared
Jan 23, 2015
SIDELAZE800 LASER BEAM DELIVERY ACCESSORY FOR CYNOSURE 1440MM WAVELENGTH LASERS
General & Plastic Surgery
228d
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