18 results
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30ms
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Sources: EU EUDAMED, US FDA
WALL BUCKY HOLDERS LT. & RT. HAND, & CENTER MOUNT
FDA 510(k)
FDA Class 1
·Radiology
INTRADUCER
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
HALOCATH LASER CATHETERS
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
FREESTYLE FREEDOM
FDA Adverse Event
Injury
·Product code NBW·February 18, 2010
3.5MM LCP ANTEROLATERAL DISTAL TIBIA PL 15 HOLES/RIGHT
FDA Adverse Event
Injury
·SYNTHES USA·Product code KTT·January 22, 2013
ENTRUST VR
FDA Adverse Event
Injury
·MEDTRONIC S.A.·Product code LWS·December 14, 2010
BIPOLAR VENTRICULAR ENDOCARDIAL LEAD
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC., CRMD·Product code DTB·July 10, 2014
ENDOLOOP LIGATURE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code GEA·December 27, 2018
MEDTRONIC LEAD
FDA Adverse Event
Death
·MEDTRONIC, INC.·Product code DXY·July 16, 2025
MEDTRONIC CRT-D
FDA Adverse Event
Death
·MEDTRONIC, INC.·Product code NIK·July 16, 2025
MEDTRONIC LEAD
FDA Adverse Event
Injury
·MEDTRONIC, INC.·Product code DXY·July 16, 2025
MEDTRONIC CRT-D
FDA Adverse Event
Injury
·MEDTRONIC, INC.·Product code NIK·July 16, 2025
FLUENCY PLUS ENDOVASCULAR STENT GRAFT
FDA Adverse Event
Injury
·ANGIOMED GMBH & CO. MEDIZINTECHNIK KG·Product code PFV·September 13, 2018
FLUENCY PLUS VASCULAR STENT GRAFT
FDA Adverse Event
Injury
·ANGIOMED GMBH & CO. MEDIZINTECHNIK KG·Product code PFV·November 19, 2019
LUMINEXX 3 VASCULAR STENT
FDA Adverse Event
Injury
·ANGIOMED GMBH & CO. MEDIZINTECHNIK KG·Product code NIO·September 13, 2018
E-LUMINEXX VASCULAR STENT
FDA Adverse Event
Injury
·ANGIOMED GMBH & CO. MEDIZINTECHNIK KG·Product code NIO·November 19, 2019
Azurion 7 M20; Catalog numbers: (1) 722079, (2) 722224, (3) 722234, (4) 722282 (OUS ONLY);
FDA Enforcement
Class I
·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·February 26, 2025
Azurion 7 M20; System Code: (1)722079, (2)722224, (3)722234, (4)722282 (OUS only);
FDA Enforcement
Class II
·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·April 8, 2026