8 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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LATITUDE ELBOW PROTHESIS
FDA 510(k)
FDA Class 2
·Orthopedic
LINEAR 3-4
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·March 2, 2021
PACING LEAD BIPOLAR ADAPTERS AND EXTENSIONS
FDA 510(k)
FDA Class 2
·Cardiovascular
VERDICT-II PROPOXYPHENE
FDA 510(k)
FDA Class 2
·Clinical Toxicology
DEPUY ASR XL FEM IMP SIZE 49
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD8010379·Product code KWA·April 22, 2013
INRATIO2
FDA Adverse Event
Malfunction
·ALERE SAN DIEGO, INC.·Product code GJS·April 15, 2011
NA
FDA Adverse Event
Malfunction
·ASCENT HEALTHCARE SOLUTIONS·Product code NLQ·July 3, 2008
Exactech Equinoxe CAGE GLENOID,POSTERIOR AUGMENT, CEMENTED, Right, Mates with: a) 38, 41, 44, 47 head, Small, Item Number 314-13-32, b) 41, 44, 47, 50, head, Medium, Item Number 314-13-33, c) 44, 47, 50, 53 head, Large, Item Number 314-13-34, d) 44, 47, 50, 53 head, Extra Large, Item Number 314-13-35; Shoulder Arthroplasty
FDA Enforcement
Class II
·Ongoing·Exactech, Inc.·April 10, 2024