10 results
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29ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Medacta Shoulder System
FDA 510(k)
FDA Class 2
·Orthopedic
REVERSE SHOULDER SYSTEM HUMERAL REVERSE HC LINER Ø42/+0MM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code PHX·July 21, 2022
REVERSE SHOULDER SYSTEM HUMERAL REVERSE HC LINER Ø39/+6MM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code PHX·December 1, 2023
SHOULDER SYSTEM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code PHX·September 30, 2025
REVERSE SHOULDER SYSTEM GLENOSPHERE 36XØ24.5
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code PHX·June 20, 2024
PATHWORK TISSUE OF ORIGIN TEST KIT-FFPE (ORIGIN TEST KIT-FFPE
FDA 510(k)
FDA Class 2
·Clinical Toxicology
SMITH & NEPHEW, INC. SURESHOT DISTAL TARGETING SYSTEM V2.0.2
FDA 510(k)
FDA Class 2
·Neurology
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
Malfunction
·INVACARE FLORIDA OPERATIONS·Product code CAW·October 22, 2014
ULTRAFLEX? ESOPHAGEAL NG
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - GALWAY·Product code ESW·June 27, 2013
B. BRAUN
FDA Adverse Event
Injury
·B. BRAUN MED. INC.·Product code NGT·March 6, 2008