11 results
·
20ms
·
Sources: EU EUDAMED, US FDA
BLADES, SCALPEL CARBON STEET
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
AXON II BRAND OF DUAL CHANNEL TENS
FDA 510(k)
FDA Class 2
·Neurology
POST-AURICULAR HEARING AID MODEL PE 600CHD
FDA 510(k)
FDA Class 1
·Ear, Nose, Throat
CAPSURE SP
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 5, 2010
RESTORE ADVANCED
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·December 3, 2012
PARADIGM INSULIN INFUSION PUMP
FDA Adverse Event
Injury
·MEDTRONIC MINIMED·Product code OYC·June 18, 2015
ARCTIC FRONT CARDIAC CRYOABLATION CATHETER
FDA Adverse Event
Death
·MEDTRONIC CRYOCATH LP·Product code OAE·July 3, 2020
HABIB ENDOHPB
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·January 30, 2023
SPACEOAR SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code OVB·September 22, 2023
ARCTIC FRONT ADVANCE CARDIAC CRYOABLATION CATHETER
FDA Adverse Event
Injury
·MEDTRONIC CRYOCATH LP·Product code OAE·July 3, 2020
SPACEOAR SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code OVB·September 12, 2022