152 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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vascuCAP
FDA 510(k)
FDA Class 2
·Radiology
Vanguard® Knee System
FDA UDI
Biomet Orthopedics, LLC·00880304270435·
OsteoMed
FDA UDI
OSTEOMED LLC·00842528128152·3.0 X 12mm Cannulated Headed Screw, T10
ELMED
FDA UDI
ELMED INCORPORATED·00842180184954·Balfour Extension, Right Side
BIOMET CC CRUCIATE TRAY 79MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·March 6, 2019
VANGUARD CR ILOK FEM-RT 70
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·March 6, 2019
MiniSPC Button
FDA UDI
APPLIED MEDICAL TECHNOLOGY, INC.·00842071148195·18F x 3.0cm MiniSPC Low Profile Suprapubic Cath...
MiniSPC Button
FDA UDI
APPLIED MEDICAL TECHNOLOGY, INC.·00842071150815·18F x 3.0cm MiniSPC Low Profile Suprapubic Cath...
BIOMET FINNED PRI STEM 40MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code HRY·October 16, 2019
BIOMET ILOK PRI TIB TRAY 75MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code HRY·October 16, 2019
EXACTECH BIOLOXDELTA / BIOLOX FEMORAL HEADS, 28MM OD, 32MM OD, 36MM OD, EXACTECH BIOLOX OPTION ADAPTERS/FEMORAL HEADS
FDA 510(k)
FDA Class 2
·Orthopedic
PAPCONE
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
InFill V2 Lateral PE
FDA UDI
PINNACLE SPINE GROUP, LLC·00814729020139·
InFill V2 Lateral PE
FDA UDI
PINNACLE SPINE GROUP, LLC·00814729020061·
InFill V2 Lateral PE
FDA UDI
PINNACLE SPINE GROUP, LLC·00814729020108·
InFill V2 Lateral PE
FDA UDI
PINNACLE SPINE GROUP, LLC·00814729020023·
XPRT SLEEP SURFACE
FDA Adverse Event
Injury
·STRYKER MEDICAL-KALAMAZOO·Product code IKZ·June 21, 2013
CARDIAC
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·October 3, 2008
AMPLATZER® SEPTAL OCCLUDER
FDA Adverse Event
Injury
·AGA MEDICAL CORPORATION·Product code MLV·July 28, 2011
VNGD CR TIB BRG 10X71/75
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·August 6, 2018