12 results
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33ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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LightWalker Laser System Family
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Edge™ Diamond PMI014-5C Pear Minimally Invasive
FDA UDI
CLINICIAN'S CHOICE DENTAL PRODUCTS, INC.·07540172002905·Diamond dental bur, reusable
IN-OVATION® Mini
FDA UDI
DENTSPLY SIRONA ORTHODONTICS INC.·D807K191552811·IN-OVATION® mini EURO 022/5-5 CS HK
IN-OVATION® Mini
FDA UDI
DENTSPLY SIRONA ORTHODONTICS INC.·D807K191552821·IN-OVATION® mini EURO 022/5-5 CBC HK
IN-OVATION® Mini
FDA UDI
DENTSPLY SIRONA ORTHODONTICS INC.·D807K191551811·IN-OVATION® mini EURO 018/5-5 CS HK
IN-OVATION® Mini
FDA UDI
DENTSPLY SIRONA ORTHODONTICS INC.·D807K191551821·IN-OVATION® mini EURO 018/5-5 CBC HK
Q-FLO CLOSED MALE LUER CONNECTOR
FDA 510(k)
FDA Class 2
·General Hospital
PHARMAPAC PERSONAL LUBRICANT
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
RESOLUTE INTEGRITY RX
FDA Adverse Event
Death
·MEDTRONIC IRELAND·Product code NIQ·October 24, 2018
MECHANICAL (MANUAL) WHEELCHAIR
FDA Adverse Event
Malfunction
·INVACARE TAYLOR STREET·Product code IOR·June 26, 2013
PLEUR-EV PE SAHARA DRY SUC/SEAL CONT REINF LF6
FDA Adverse Event
Malfunction
·TELEFLEX MEDICAL·Product code BTR·July 20, 2011
ELECSYS 2010 DISK
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code MMI·September 26, 2008