22 results
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20ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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KSEA UNIVERSAL LAPAROMAT LAPAROSCOPIC SUCTION AND IRRIGATION PUMP
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Endo Carry-on Procedure Kit
FDA UDI
MEDIVATORS INC.·00677964151293·Endo Carry-on Procedure Kit contains Basin, VIA...
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450128503·
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450051573·
WERNER HARFMANN GMBH
FDA registration
WERNER HARFMANN GMBH·6 products·🇩🇪 Germany
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033173411·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033173398·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033173435·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033173374·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033173404·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033173428·
RESTORE
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·October 2, 2013
RADIESSE DERMAL FILLER
FDA Adverse Event
Injury
·BIOFORM MEDICAL, INC.·Product code LMH·April 10, 2009
INFINITY AMYLASE REAGENT (PROCEDURE NO. 580/568)
FDA 510(k)
FDA Class 2
·Clinical Chemistry
DURABOND NON-PRECIOUS CERAMIC ALLOY
FDA 510(k)
FDA Class 2
·Dental
NATURALYTE
FDA Adverse Event
Death
·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·March 15, 2013
SYNCHROMED II
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LKK·March 1, 2011
ATLAS + VR
FDA Adverse Event
Malfunction
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NIK·March 10, 2008
BACFIX ROD, UNKNOWN
FDA Adverse Event
Injury
·ZIMMER BIOMET SPINE INC.·Product code HSB·January 16, 2020
Upper roller bracket (part number 1088370) for the Gen2 gantry enclosure for the Radixact Treatment Delivery System.
FDA Enforcement
Class II
·Completed·Accuray Incorporated·September 6, 2023