20 results
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23ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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AMERIWATER OZONE DISINFECTION SYSTEM
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04051526550179·GENUMEDI PT KNEE SUP SILVER R EW III
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04051526550124·GENUMEDI PT KNEE SUP SILVER L EW III
Biomet® Knee System
FDA UDI
Biomet Orthopedics, LLC·00887868558511·
Biomet® Knee System
FDA UDI
Biomet Orthopedics, LLC·00887868247781·
BIOMET KNEE SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304005433·
3M™ Unitek™
FDA UDI
3M UNITEK CORPORATION·00652221037008·Unitek(TM) Bicuspid Band General Purpose Narrow...
Kirwan
FDA UDI
KIRWAN SURGICAL PRODUCTS LLC·00841019103548·Non-Stick Bipolar Coagulation Forceps 7 1/2" (1...
Sage Cervical Interbody Fusion System
FDA UDI
CURITEVA, INC.·B648C21414121370·Titanium Cervical Spacer, 14 x 12 x 13mm, 7 deg
Sage Cervical Interbody Fusion System
FDA UDI
CURITEVA, INC.·B648C2241412137CT0·PEEK Cervical Spacer with Titanium Plasma Coati...
GRANDIO FLOW
FDA 510(k)
FDA Class 2
·Dental
3DSCOPE
FDA 510(k)
FDA Class 2
·Radiology
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 3, 2014
STERRAD® CYCLESURE® 24 BIOLOGICAL INDICATOR
FDA Adverse Event
Malfunction
·ADVANCED STERILIZATION PRODUCTS·Product code FRC·June 3, 2013
ANEURX STENT GRAFT SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC CARDIOVASCULAR·Product code MIH·June 22, 2011
PALACOS R 1X40 SINGLE
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LOD·April 21, 2022
PALACOS R 1X40 SINGLE
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LOD·April 21, 2022
MICROVASCULAR PLUG
FDA Adverse Event
Injury
·REVERSE MEDICAL·Product code KRD·September 8, 2021
MICROVASCULAR PLUG
FDA Adverse Event
Injury
·REVERSE MEDICAL·Product code KRD·September 8, 2021
ESOPHYX Z
FDA Adverse Event
Injury
·ENDOGASTRIC SOLUTIONS, INC.·Product code ODE·June 22, 2017