11 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
3M DENT II SYSTEM
FDA 510(k)
FDA Class 2
·Dental
Polystar Selection EDITION
FDA UDI
Merz Dental GmbH·D7091981647·anteriors; shade D2 light; mould US2
ELECTROSURGICAL PENCIL WITH PTFE COATED & UNCOATED ELECTRODE TIPS
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Bandit guidewire
FDA 510(k)
FDA Class 2
·Cardiovascular
AIRVANCE BONE SCREW (REPOSE) SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC XOMED INC.·Product code LRK·March 3, 2014
AIRVANCE BONE SCREW (REPOSE) SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC XOMED, INC·Product code LRK·March 29, 2013
ROTABLATOR ROTATIONAL ATHERECTOMY SYSTEM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - FREMONT (CE)·Product code MCX·February 27, 2013
TRIDENT 0 DEG CONSTRAINED INSERT 28G
FDA Adverse Event
Malfunction
·STRYKER ORTHOPAEDICS MAHWAH·Product code KWZ·January 12, 2011
EMAX 2 MOTOR
FDA Adverse Event
Malfunction
·DEPUY SYNTHES POWER TOOLS·Product code HBC·December 18, 2013
AIRVANCE¿ THS SYSTEM - BONE SCREW WITH SUTURE
FDA Adverse Event
Injury
·MEDTRONIC XOMED INC.·Product code LRK·November 30, 2015
AIRVANCE¿ THS SYSTEM - TOUNGE SUSPENSION KIT
FDA Adverse Event
Malfunction
·MEDTRONIC XOMED INC.·Product code LRK·October 2, 2015