47 results
·
22ms
·
Sources: EU EUDAMED, US FDA
CAREO SAFETY SYRINGE FOR U-100 INSULIN 0.5CC/ML
FDA 510(k)
FDA Class 2
·General Hospital
Paltop
FDA UDI
PALTOP ADVANCED DENTAL SOLUTIONS LTD·07290108694635·3mm Conical Non-Engage Ti Base Abutment
LIFECORE BIOMEDICAL DENTAL IMPLANT SYSTEMS
FDA 510(k)
FDA Class 2
·Dental
HEALTHLIFE OXYGEN CONCENTRATOR MODEL AS009
FDA 510(k)
FDA Class 2
·Anesthesiology
36MM COCR BIOMET FEM HD STD NK
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code KWA·June 13, 2016
UNKNOWN EXCEED HIP
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code KWA·August 5, 2016
UNKNOWN RECAP 48MM HEAD
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code KWA·September 16, 2016
36MM 12/14 TPR FEM HEAD -4 NK
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code KWA·June 28, 2016
EXCEED ABT M2A-36 MOD HEAD
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code KWA·June 28, 2016
EXCEED ABT RINGLOC-X SHELL
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code KWA·July 20, 2017
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·March 27, 2025
M2A MOD HD COCR DIA28/+3MM T1
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code KWA·December 23, 2015
32MM COCR BIOMET FEM HD STD NK
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code KWA·February 16, 2016
RECAP/MAGNUM ACETABULAR SHELL
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code KWA·February 15, 2017
EXCEED ABT M2A-36 MOD HEAD -3MM T1
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code KWA·June 1, 2016
COULTER® LH 750 HEMATOLOGY ANALYZER
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code GKZ·April 22, 2013
LTV
FDA Adverse Event
Malfunction
·CAREFUSION 203, INC.·Product code CBK·April 20, 2011
SIGMA 300 D
FDA Adverse Event
Injury
·MEDTRONIC S.A.·Product code DXY·July 10, 2008
RECAP SHELL COCR PC DIA56/50MM
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code KWA·September 1, 2016
36MM COCR BIOMET FEM HD +6 NK
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code KWA·September 7, 2018