109 results · 37ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

CUTERA, INC.

FDA Adverse Event
Injury ·CUTERA, INC.·Product code GEX·December 2, 2008

ENLIGHTEN III

FDA Adverse Event
Injury ·CUTERA, INC.·Product code GEX·May 23, 2025

TRUSCULPT ID

FDA Adverse Event
Injury ·CUTERA, INC.·Product code GEI·June 10, 2025

CUTERA XEO LASER

FDA Adverse Event
Malfunction ·CUTERA, INC.·Product code GEX·May 5, 2012

GENESIS V

FDA Adverse Event
Injury ·CUTERA, INC·Product code GEX·December 15, 2016

LASER GENESIS

FDA Adverse Event
Injury ·CUTERA, INC.·Product code GEX·May 8, 2014

TRUSCULPT

FDA Adverse Event
CUTERA, INC.·Product code PBX·October 10, 2014

ENLIGHTEN

FDA Adverse Event
Injury ·CUTERA, INC·Product code GEX·October 25, 2017

ENLIGHTEN

FDA Adverse Event
Injury ·CUTERA, INC·Product code GEX·October 26, 2017

TRUSCULPT 3D

FDA Adverse Event
Injury ·CUTERA INC·Product code PBX·May 21, 2021

TRUSCULPT ID

FDA Adverse Event
Injury ·CUTERA, INC.·Product code PBX·June 7, 2022

TRUSCULPT

FDA Adverse Event
Injury ·CUTERA, INC.·Product code NUV·June 13, 2012

TRUSCULPT ID

FDA Adverse Event
Injury ·CUTERA, INC.·Product code PBX·June 7, 2022

TITAN XL

FDA Adverse Event
Other ·CUTERA, INC.·Product code ILY·February 17, 2012

TRUSCULPT ID

FDA Adverse Event
Injury ·CUTERA, INC.·Product code GEI·September 10, 2024

TRUSCULPT ID

FDA Adverse Event
Injury ·CUTERA, INC.·Product code GEI·July 5, 2024

LIMELIGHT

FDA Adverse Event
Injury ·CUTERA, INC.·Product code ILY·July 1, 2024

TRUSCULPT ID

FDA Adverse Event
Injury ·CUTERA, INC.·Product code GEI·July 23, 2024

ENLIGHTEN III

FDA Adverse Event
Injury ·CUTERA, INC.·Product code GEX·July 6, 2024

EXCEL V

FDA Adverse Event
Malfunction ·CUTERA, INC·Product code GEX·February 12, 2013