21 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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EBA One Nailing System
FDA 510(k)
FDA Class 2
·Orthopedic
Vanguard® Knee System
FDA UDI
Biomet Orthopedics, LLC·00880304272040·
Vanguard Knee System
FDA UDI
Biomet Orthopedics, LLC·00880304466135·
XIA 3 SPINAL SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
LANX LATERAL
FDA 510(k)
FDA Class 2
·Orthopedic
FMRL PS OPEN INTL LT
FDA Adverse Event
Injury
·BIOMET INC.·Product code JWH·February 6, 2020
OCTRODE LEAD KIT, 60CM LENGTH
FDA Adverse Event
Injury
·ABBOTT MEDICAL·Product code LGW·June 16, 2024
INTERSTIM II
FDA Adverse Event
Malfunction
·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code EZW·July 8, 2011
BEND-SCR F/UNILOCK-RECOPL TI
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code LXH·June 22, 2013
FLO-GARD 6201 VOLUMETRIC INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE·Product code FRN·October 4, 2008
UNKNOWN CEMENT
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LOD·March 20, 2020
BIOMET ARCOM PATELLA
FDA Adverse Event
Death
·ZIMMER BIOMET, INC.·Product code JWH·November 8, 2018
BIOMET CC CRUCIATE TRAY
FDA Adverse Event
Death
·ZIMMER BIOMET, INC.·Product code JWH·November 7, 2018
VANGUARD PS INTERLOCKING FEMORAL
FDA Adverse Event
Death
·ZIMMER BIOMET, INC.·Product code JWH·November 8, 2018
VANGUARD TM PS OPEN BOX FEMORAL - 72.5 MM LEFT-INTERLOK
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JWH·May 5, 2017
BIOMET FIXED I-BEAM TIBIAL PLATE INTERLOK - WITH LOCKING BAR
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JWH·May 5, 2017
VANGUARD SERIES-A STANDARD PATELLA ARCOM THREE 1/4" PEGS
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JWH·May 5, 2017
UNKNOWN FEMORAL COMPONENT
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·March 20, 2020
SERIES A ASYMMETRIC PAT 34X8.5
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·March 20, 2020
BIOMET CC CRUCIATE TRAY 79MM MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·March 20, 2020