9 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ACE BONE SCREW TACKING KIT
FDA 510(k)
FDA Class 2
·Dental
DeBakey Vascular Clamps
FDA UDI
KOROS U.S.A., INC.·10840199540034·DeBakey Vascular Clamps Accutely Curved 9cm Jaw...
SIGNAL MEDICAL CORPORATION BEACON KNEE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
Symani Surgical System
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
AMIS 01.15.10.0321 AMIS SOCK SINGLE USE
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LXH·November 25, 2021
AMIS SHOE
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LXH·December 3, 2021
PULSE-GENERATOR, PACEMAKER, EXTERNAL
FDA Adverse Event
Malfunction
·MEDTRONIC MILACA, INC.·Product code DTE·February 9, 2013
TELIGEN
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code LWS·January 6, 2011
1288 CCU WITH FIBER BOARD INTERNATIONAL KIT
FDA Adverse Event
Malfunction
·STRYKER ENDOSCOPY-SAN JOSE·Product code GCJ·July 23, 2014