13 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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PreXion3D Excelsior
FDA 510(k)
FDA Class 2
·Radiology
OSTEOTRANS -MX BIOABSORBABLE BONE FIXATION SYSTEM
FDA 510(k)
FDA Class 2
·Dental
VIRTUE MALE SLING SYSTEM AND ALEXIS(R) WOUND RETRACTOR KIT
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
SYSTEM, PERITONEAL, AUTOMATIC DELIVERY
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE·Product code FKX·June 11, 2013
PINN CAN BONE SCREW 6.5MMX50MM
FDA Adverse Event
Injury
·DEPUY-RAYNHAM, A DIVISION OF DEPUY ORTHPAEDICS, INC.·Product code NDJ·July 11, 2011
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·October 10, 2014
SHORELINE ACS, WAVEFORM C
FDA Adverse Event
Injury
·SEASPINE ORTHOPEDICS CORPORATION·Product code OVE·November 12, 2025
SHORELINE ACS, WAVEFORM C
FDA Adverse Event
Injury
·SEASPINE ORTHOPEDICS CORPORATION·Product code OVE·November 12, 2025
SHORELINE ACS, WAVEFORM C
FDA Adverse Event
Injury
·SEASPINE ORTHOPEDICS CORPORATION·Product code OVE·November 12, 2025
CROSSCATH SUPPORT CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code KRA·March 6, 2019
CROSSCATH SUPPORT CATHETER
FDA Adverse Event
Injury
·COOK INC·Product code KRA·February 26, 2019
CROSSCATH SUPPORT CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code KRA·June 20, 2019
OMNIPOD 5 APP
FDA Adverse Event
Injury
·INSULET CORPORATION·Product code QFG·March 10, 2023