16 results
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21ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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BIVONA AIRE-CUF TRACHEOSTOMY TUBE W/TALK ATTACH.
FDA 510(k)
FDA Class 2
·Anesthesiology
PORTEX® BIVONA® AIRE-CUF® ADULT TRACHEOSTOMY TUBES
FDA Adverse Event
Malfunction
·SMITHS MEDICAL ASD INC.·Product code JOH·September 1, 2016
PORTEX® BIVONA® AIRE-CUF® ADULT TRACHEOSTOMY TUBES
FDA Adverse Event
Malfunction
·SMITHS MEDICAL ASD INC.·Product code JOH·September 1, 2016
MODIFICATION TO FIXION INTERLOCKING PROXIMAL FEMORAL INTRAMEDULLARY NAILING SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
PMMA CAD/CAM DISC
FDA 510(k)
FDA Class 2
·Dental
REVERSE SHOULDER SYSTEM HUMERAL REVERSE HC LINER Ø42/+0MM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code PHX·July 21, 2022
TAPERLOC FEMORAL STEM
FDA Adverse Event
Injury
·BIOMET UK LTD·Product code LPH·December 2, 2010
ON-Q PAIN PUMP
FDA Adverse Event
Injury
·I-FLOW, LLC·Product code MEB·January 9, 2013
FOUNDATION KNEE
FDA Adverse Event
Injury
·ENCORE MEDICAL, L.P.·Product code JWH·July 3, 2014
TPRLC 133 T1 PPS HO 11X142MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LZO·January 4, 2024
CER BIOLOXD OPTION HD 36MM
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LZO·January 9, 2024
G7 NEUTRAL E1 LINER 36MM F
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code PBI·January 4, 2024
G7 FINNED 4 HOLE SHELL 56F
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·January 4, 2024
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