10 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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TDM Large Bone Plate and Screw System
FDA 510(k)
FDA Class 2
·Orthopedic
Capo Slow Flow capsules clear, 20 x 0.25
FDA UDI
Schütz Dental GmbH·ESDG2321151·Capo Slow Flow is a light-curing, flowable, hig...
ABSOLUTE DENTIN 2
FDA 510(k)
FDA Class 2
·Dental
NEUROLAC NERVE GUIDE MODELS NG01-15/03, NG01-020/03, NG01 025/03, NG01-030/03
FDA 510(k)
FDA Class 2
·Neurology
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·August 21, 2025
LIFEPAK 20 DEFIBRILLATOR/MONITOR
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC.·Product code LDD·November 4, 2008
UNICEL® DXC 600I SYNCHRON® ACCESS® CLINICAL SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code JJE·September 1, 2011
PRISMAFLEX
FDA Adverse Event
Injury
·GAMBRO LUNDIA AB·Product code KDI·July 17, 2013
POSITION-PIN 4.5 F/LCP TI
FDA Adverse Event
Injury
·SYNTHES SELZACH·Product code HWC·February 2, 2017
INTELLIVUE PATIENT MONITOR MX750
FDA Adverse Event
Death
·PHILIPS MEDIZIN SYSTEME BÖBLINGEN GMBH·Product code MHX·August 15, 2025