8 results
·
22ms
·
Sources: EU EUDAMED, US FDA
NEW DOUBLO 2.0
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
NA
FDA UDI
aap Implantate AG·04042409445507·Cannulated Headless Bone Screw 2.5, L 34, TL 13...
TERASON ULTRASOUND SYSTEM WITH CONTINUOUS WAVE SOPPLER
FDA 510(k)
FDA Class 2
·Radiology
Keystone Dental XL Dental Implant System
FDA 510(k)
FDA Class 2
·Dental
SCISSORS, POINTED, 5 FR., 34 CM
FDA Adverse Event
Malfunction
·KARL STORZ SE & CO. KG·Product code GCJ·July 31, 2025
PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM
FDA Adverse Event
Injury
·ABBOTT VASCULAR - REDWOOD CITY·Product code MGB·December 3, 2008
ENDEAVOR RX CORONARY STENT SYSTEM
FDA Adverse Event
Death
·MEDTRONIC IRELAND·Product code NIQ·September 13, 2011
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 29, 2013