8 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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DYONICS VARICOSE VEIN ABLATION BLADE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
PROPHYLAXIS CUPS AND POLISHERS
FDA 510(k)
FDA Class 1
·Dental
HEX-LOCK SHORT ABUTMENT, MODEL SA341, SA342, SA451, SA452, SA561, SA562 SHORT HEALING CAP, MODEL SAHEAL4, SAHEAL5,
FDA 510(k)
FDA Class 2
·Dental
NEUROMONITOR BASIC KIT
FDA Adverse Event
Malfunction
·INTEGRA LIFESCIENCES SWITZERLAND SAR·Product code GWM·November 9, 2022
MAINFRAME 8253001 NIM RESPONSE 3.0
FDA Adverse Event
Injury
·MEDTRONIC XOMED, INC·Product code ETN·November 7, 2013
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
Malfunction
·INVACARE FLORIDA OPERATIONS·Product code CAW·March 5, 2013
CAPSUREFIX NOVUS
FDA Adverse Event
Malfunction
·MEDTRONIC SINGAPORE OPERATIONS·Product code DTB·August 8, 2014
LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM 10.0CM
FDA Adverse Event
Injury
·ALLERGAN·Product code LTI·February 8, 2011