8 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CORFLO CUBBY LOW PROFILE GASTROSTOMY DEVICE (LPGD)
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Eargo 5
FDA UDI
Eargo, Inc.·00850010429236·Right Eargo 5 Hearing Device
Reprocessed Livewire Steerable Diagnostic Electrophysiology Catheter
FDA 510(k)
FDA Class 2
·Cardiovascular
METATARSAL DECOMPRESSION IMPLANT, MODEL 100
FDA 510(k)
FDA Class 2
·Orthopedic
INSERT, BIPOLAR FORCEPS
FDA Adverse Event
Malfunction
·RICHARD WOLF MEDICAL INSTRUMENTS CORP.·Product code GEI·April 2, 2015
RX CYTOLOGY BRUSH
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - SPENCER·Product code FDX·March 5, 2013
SPRINT QUATTRO SECURE
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO, INC.·Product code LWS·February 15, 2011
CONSULTA CRT-D
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NIK·August 7, 2014