46 results
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24ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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iHealth Infrared No-Touch Forehead Thermometer
FDA 510(k)
FDA Class 2
·General Hospital
ELMED
FDA UDI
ELMED INCORPORATED·00842180102675·MONOPOLAR RF-CABLE WITH FEMALE BANANA (4 MM DIA...
METZENBAUM SCISSORS
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896055292·METZENBAUM SCISSORS CURVED TUNGSTEN CARBIDE BLA...
IN-OVATION® C
FDA UDI
DENTSPLY SIRONA ORTHODONTICS INC.·D807K100531101·IN-OVATION® C Base Rx 018 U5-5/L3-3 CS HK
IN-OVATION® C
FDA UDI
DENTSPLY SIRONA ORTHODONTICS INC.·D807K100531601·IN-OVATION® C Roncone 018 U5-5/L3-3 CS HK
IN-OVATION® C
FDA UDI
DENTSPLY SIRONA ORTHODONTICS INC.·D807K100531111·IN-OVATION® C Base Rx 018 U5-5/L3-3 CS-BC HK
IN-OVATION® C
FDA UDI
DENTSPLY SIRONA ORTHODONTICS INC.·D807K100531001·IN-OVATION® C Base Rx 018 U5-5/L3-3
IN-OVATION® C
FDA UDI
DENTSPLY SIRONA ORTHODONTICS INC.·D807K100531611·IN-OVATION® C Roncone 018 U5-5/L3-3 CS-BC HK
PHILIPS MULTI-PARAMETER MODULE, MODEL M3001A; PHILIPS COMPONENT COMPACT MONITOR, RELEASE A.02, MODEL M1275B
FDA 510(k)
FDA Class 2
·Cardiovascular
VISCOPE, MODEL 100P,100S
FDA 510(k)
FDA Class 2
·Cardiovascular
DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·July 28, 2025
HYLAFORM
FDA Adverse Event
Injury
·GENZYME BIOSURGERY·Product code LMH·March 14, 2006
ACRYSOF
FDA Adverse Event
Injury
·ALCON RESEARCH, LTD. / HUNTINGTON·Product code HQL·March 13, 2009
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code OYC·October 24, 2014
MAXIMO VR
FDA Adverse Event
Injury
·MEDTRONIC MED REL, INC.·Product code LWS·August 11, 2011
MECHANICAL WALKER, ROLLATOR
FDA Adverse Event
DANYANG MAXTHAI MEDICAL EQUIPMENT·Product code ITJ·July 1, 2013
2520274-2013-06222
FDA Adverse Event
Injury
·SYNTHES USA·Product code HSB·September 6, 2013
2520274-2013-06219
FDA Adverse Event
Injury
·SYNTHES USA·Product code HSB·September 6, 2013
ACRYSOF
FDA Adverse Event
Injury
·ALCON RESEARCH, LTD. / HUNTINGTON·Product code HQL·March 13, 2009
2520274-2013-06221
FDA Adverse Event
Injury
·SYNTHES USA·Product code HSB·September 6, 2013