25 results
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39ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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ERCHONIA PL2000
FDA 510(k)
FDA Class 2
·Physical Medicine
Graftmaster
FDA UDI
ABBOTT VASCULAR INC.·08717648176357·GRAFTMASTER Coronary Stent Graft System 2.80 mm...
Graftmaster
FDA UDI
ABBOTT VASCULAR INC.·08717648176364·GRAFTMASTER Coronary Stent Graft System 2.80 mm...
Graftmaster
FDA UDI
ABBOTT VASCULAR INC.·08717648176340·GRAFTMASTER Coronary Stent Graft System 2.80 mm...
STEVE MADDEN
FDA UDI
FGX INTERNATIONAL INC.·00193033427552·
STEVE MADDEN
FDA UDI
FGX INTERNATIONAL INC.·00193033427576·
STEVE MADDEN
FDA UDI
FGX INTERNATIONAL INC.·00193033427569·
PedFuse®
FDA UDI
SPINEFRONTIER, INC.·00190361011873·PedFuse Respond, CNL, 9.0mm x 80mm
PRAIRIE CRUISER
FDA 510(k)
FDA Class 2
·Physical Medicine
PALOMAR SLP 1000
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
GRAFTMASTER RX CORONARY STENT GRAFT SYSTEM
FDA Adverse Event
Injury
·ABBOTT VASCULAR·Product code MAF·July 28, 2020
GRAFTMASTER RX CORONARY STENT GRAFT SYSTEM
FDA Adverse Event
Injury
·ABBOTT VASCULAR·Product code MAF·February 9, 2021
GRAFTMASTER RX CORONARY STENT GRAFT SYSTEM
FDA Adverse Event
Injury
·ABBOTT VASCULAR·Product code MAF·September 16, 2021
ACCU-CHEK ® SPIRIT
FDA Adverse Event
Malfunction
·ROCHE DIABETES CARE AG·Product code LZG·March 20, 2013
ASR ACETABULAR CUPS 52
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL, LTD.·Product code KWA·February 24, 2011
JOURNEY BCS
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC./ORTHOPAEDIC DIV.·Product code HSH·March 12, 2008
GRAFTMASTER
FDA Adverse Event
Malfunction
·ABBOTT VASCULAR INC.·Product code MAF·April 1, 2024
ULTRACISION HARMONIC ACE (EXACT CODE UNKNOWN)
FDA Adverse Event
Injury
·ETHICON ENDO-SURGERY, LLC.·Product code LFL·December 6, 2019
M2A-MAGNUM PF CUP 56ODX50ID
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·February 22, 2022
GRAFTMASTER RX CORONARY STENT GRAFT SYSTEM
FDA Adverse Event
Malfunction
·ABBOTT VASCULAR·Product code MAF·July 9, 2020