150 results
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24ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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JUSHA-M53 Medical Display
FDA 510(k)
FDA Class 2
·Radiology
AGXO
FDA UDI
Oticon A/S·05707131280923·H160V2, BTE 13 WL 100 CBE AGXO
BIOMET KNEE SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304005174·
Biomet® Knee System
FDA UDI
Biomet Orthopedics, LLC·00887868344374·
PTA-PLUS PTA BALLOON CATHER 5 MM X 4CM, PTA-PLUS PTA BALLOON CATHETER 6MM X 4CM
FDA 510(k)
FDA Class 2
·Cardiovascular
AGCEL WOUND DRESSING,AGCEL BURN DRESSING
FDA 510(k)
FDA Unclassified
·Unknown
VANGUARD DCM PS TIBIBAL BEARING 14MM X 71/75MM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JWH·February 10, 2017
ASCENT PRI LIP BRG 12X71/75
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code HRY·July 1, 2021
BIOMET
FDA Adverse Event
Injury
·BIOMET ORTHOPAEDICS, INC.·Product code HSA·June 26, 2008
ASCENT PRI INLK FMRL MED LT
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code HRY·July 1, 2021
DCM VANGUARD CR TIBIAL BEARING 10MM X 71/75MM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JWH·December 6, 2016
VANGUARD CR FEMORAL 67.5MM RIGHT ¿ INTERLOK - DEVIATION
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JWH·December 6, 2016
BIOMET INTERLOK 75MM FIXED CRUCIATE TIBIAL PLATE WITH LOCKING BAR
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JWH·December 6, 2016
BMET ARCOM AP PAT 3PST 34MM MD
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·July 1, 2021
BIOMET CC I-BEAM TRAY 75MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code HRY·July 1, 2021
WALLSTENT RP ENDOPROSTHESIS
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code JCT·March 21, 2025
MAXIM PRIMARY LIPPED TIBIAL BEARING 12 MM THICK X 63/67 MM WIDE
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JWH·February 24, 2017
INSIGNIA
FDA Adverse Event
Malfunction
·GUIDANT CRM CLONMEL IRELAND·Product code LWP·October 8, 2014
AC-POWERED ADJUSTABLE HOSPITAL BED, INCLUDING RAILS
FDA Adverse Event
Malfunction
·CARROLL HEALTHCARE·Product code FNL·June 6, 2013
FINELINE II
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code NVN·July 6, 2011