11 results
·
28ms
·
Sources: EU EUDAMED, US FDA
HYDROX STERILE WATER 4 OZ. CUP 120 ML., HYDROX STERILE WATER 100 ML BOTTLE
FDA 510(k)
FDA Class 2
·General Hospital
DANTEC 13L40 ST. MARKS'S PUDENDAL ELECTRODE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
CARDIOFAX ECG-8830A
FDA 510(k)
FDA Class 2
·Cardiovascular
PSO KNEE BONE SUBSTITUTION
FDA Adverse Event
Injury
·BIOMET SPAIN, S.L.·Product code KRO·April 22, 2022
PROFILE BIABUT 4.0 -Ø5.5
FDA Adverse Event
Injury
·DENTSPLY IMPLANTS MANUFACTURING GMBH·Product code DZE·February 24, 2026
PSO KNEE BONE SUBSTITUTION
FDA Adverse Event
Injury
·BIOMET SPAIN, S.L.·Product code KRO·July 18, 2019
POSEY KEEPSAFE DELUXE
FDA Adverse Event
Malfunction
·J. T. POSEY CO.·Product code KMI·January 18, 2013
PRECISION TEST STRIPS
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE, INC. USA·Product code NBW·January 31, 2011
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
Malfunction
·INVACARE FLORIDA OPERATIONS·Product code CAW·August 4, 2014
UNKNOWN HEAD
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·February 16, 2018
STANMORE ACET CUP ARCOM 28X50
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDI·March 18, 2020