46 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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NOVATION INTEGRIP ACETABULAR AUGMENTS, GROUPS 4 AND 5
FDA 510(k)
FDA Class 2
·Orthopedic
Comprehensive® Shoulder System
FDA UDI
Biomet Orthopedics, LLC·00887868267598·
COMPREHENSIVE SHOULDER SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304554108·
N/A
FDA UDI
HANS RUDOLPH, INC.·00874750003952·75 V2 PETITE 22ID STRAGHT NOHG
EPIDUCER LEAD DELIVERY SYSTEM
FDA 510(k)
FDA Class 2
·Neurology
NEXUS 2 CLEAR
FDA 510(k)
FDA Class 2
·Dental
EQUINOXE
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code KWT·September 13, 2019
COMPREHENSIVE REVERSE SHOULDER GLENOSPHERE MINI BASEPLATE WITH TAPER ADAPTER
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWS·December 1, 2016
COMPREHENSIVE REVERSE SHOULDER 6.5MM CENTRAL SCREW
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code PAO·December 1, 2016
FIXED LOCKING SCREW 3.5 HEX
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code PAO·December 1, 2016
FIXED LOCKING SCREW 3.5 HEX
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code PAO·December 1, 2016
FIXED LOCKING SCREW 3.5 HEX
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code PAO·December 1, 2016
IMPAX CV OUTBOUND (RESULTS MANAGEMENT 2.08)
FDA Adverse Event
Malfunction
·AGFA HEALTHCARE CORP·Product code LLZ·February 28, 2014
M2A-MAGNUM 42-50MM TPR INSRT-6
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·May 15, 2013
INRATIO
FDA Adverse Event
Malfunction
·ALERE SAN DIEGO, INC.·Product code GJS·May 24, 2011
EQUINOXE
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code KWT·February 6, 2019
EQUINOXE
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code KWT·November 3, 2021
OCTRODE LEAD KIT, 60CM LENGTH
FDA Adverse Event
Injury
·ABBOTT MEDICAL·Product code LGW·September 9, 2022
EQUINOXE
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code KWT·July 29, 2019
EQUINOXE
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code KWT·December 26, 2019