9 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
TRAUMA PAD 5 X 9
FDA 510(k)
FDA Unclassified
·Unknown
VARIAX
FDA UDI
Stryker GmbH·07613327177244·Wrist Tray Clip
N/A
FDA UDI
Tyber Medical, LLC·M695M9403480·
MODIFICATION TO HNC-127-INT NEUROVASCULAR ARRAY COIL
FDA 510(k)
FDA Class 2
·Radiology
INTERBODY CAGE
FDA 510(k)
FDA Class 2
·Orthopedic
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code KWP·February 3, 2013
PIONEER MATTRESS 30"
FDA Adverse Event
Malfunction
·STRYKER CORP., MEDICAL DIVISION·Product code IKY·December 9, 2010
ARTICULEZE M HEAD 36MM +5
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code JDI·July 17, 2014
Captus 4000e Thyroid Uptake System, Model Numbers 5430-30151 and 5430-30152 - Product Usage: is intended to be used by trained nuclear Medicine Technologists or Nuclear Medicine Physicians to perform Thyroid Uptake Procedures.
FDA Enforcement
Class II
·Terminated·Capintec Inc·April 1, 2020