9 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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PARTIAL & TOTAL OSSICULAR REPLACEMENT PROSTHESIS
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
N/A
FDA UDI
MEDTRONIC NAVIGATION, INC.·00673978963204·ACC 963-752 CLAMPING RING ZEIHM 9 II
Needle Holder
FDA UDI
KATENA PRODUCTS, INC.·00841668108383·ANIS NEEDLE HOLDER CURVED WITH LOCK
VALTRAC (BAR) REMOVER DEVICE
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
LIFESENSE, MODEL LS1-9R
FDA 510(k)
FDA Class 2
·Cardiovascular
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 7, 2014
SOLYX SIS SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·February 15, 2013
ECHELON*FLEX60
FDA Adverse Event
Injury
·ETHICON ENDO SURGERY, INC (CINCINNATI)·Product code GDW·January 19, 2011
2.5 mm Reaming Rod W/Ball Tip 650 mm, Sterile
FDA Enforcement
Class II
·Terminated·Synthes (USA) Products LLC·November 30, 2016