21 results · 35ms · Sources: EU EUDAMED, US FDA

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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