21 results
·
35ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
COMFORT WEAR
FDA Adverse Event
Death
·THE MARENA GROUP, INC.·Product code MDR·March 26, 2003
FLOWTRON EXCEL
FDA Adverse Event
Injury
·HUNTLEIGH HEALTHCARE·Product code JOW·January 9, 2003
RENUVION
FDA Adverse Event
Injury
·APYX MEDICAL CORPORATION·Product code GEI·July 2, 2024
RENUVION
FDA Adverse Event
Injury
·APYX MEDICAL CORPORATION·Product code GEI·February 27, 2026
MEROCEL SURGIAL PRODUCTS
FDA Adverse Event
Injury
·MEROCEL SURGICAL PRODUCTS·Product code FRL·February 13, 2001
RENUVION APR HANDPIECE
FDA Adverse Event
Injury
·APYX MEDICAL CORPORATION·Product code GEI·March 29, 2024
RENUVION
FDA Adverse Event
Injury
·APYX MEDICAL CORPORATION·Product code GEI·January 12, 2022
AVELI
FDA Adverse Event
Injury
·REVELLE AESTHETICS, INC.·Product code OUP·June 29, 2022
RENUVION® APR HANDPIECE
FDA Adverse Event
Injury
·APYX MEDICAL CORPORATION·Product code GEI·August 6, 2024
RENUVION
FDA Adverse Event
Injury
·APYX MEDICAL CORPORATION·Product code GEI·February 16, 2022
RENUVION
FDA Adverse Event
Injury
·APYX MEDICAL CORPORATION·Product code GEI·September 24, 2022
VASERLIPO SYSTEM
FDA Adverse Event
Injury
·SOLTA MEDICAL, INC·Product code MUU·September 22, 2022
STRATAFIX SPIRAL MONOCRYL PLUS UNKNOWN
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAM·February 3, 2026
VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAM·February 3, 2026
VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAM·February 3, 2026
STRATAFIX SPIRAL MONOCRYL PLUS UNKNOWN
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAM·February 3, 2026
VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAM·February 3, 2026
VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAM·February 3, 2026
INTERSTIM II
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code EZW·October 2, 2018
CANNULA
FDA Adverse Event
Injury
·Product code MUU·September 17, 2014