8 results
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26ms
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Sources: EU EUDAMED, US FDA
ELECSYS PSA, MODEL 2010
FDA 510(k)
FDA Class 2
·Immunology
Healix Compression Screw System
FDA 510(k)
FDA Class 2
·Orthopedic
ORTHOPEDIATRICS BONE SCREWS
FDA 510(k)
FDA Class 2
·Orthopedic
VASOVIEW HEMOPRO 2
FDA Adverse Event
Malfunction
·MAQUET CARDIOVASCULAR, LLC·Product code GEI·February 22, 2013
FREESTYLE FREEDOM LITE
FDA Adverse Event
Injury
·Product code NBW·February 9, 2011
TRILOGY O2
FDA Adverse Event
Malfunction
·RESPIRONICS INC.,·Product code CBK·July 2, 2014
Exactech Equinoxe REVERSE SHOULDER,42mm Constrained Humeral Liner, a) +0mm, Item number 320-42-10, b) +2.5mm, Item Number 320-42-13; Shoulder Arthroplasty
FDA Enforcement
Class II
·Ongoing·Exactech, Inc.·April 10, 2024
Assurity Model Numbers: PM1240, PM2240; Assurity + Model Number: PM2260; Accent Model Numbers: PM1210, PM2210, PM1222, PM2212; Accent MRI Model Numbers: PM1224, PM2218, PM2224 Implantation of a single-chamber pulse generator, dual-chamber pulse generator, or CRT-P is indicated in one or more of the following permanent conditions: Syncope, Presyncope, Fatigue, Disorientation, Or any combination of those symptoms. Implantation of a CRT-P is indicated for: Maintaining synchrony of the left and right ventricles in patients who have undergone an AV nodal ablation for chronic atrial fibrillation and have NYHA Class II or III heart failure. The reduction of the symptoms of moderate to severe heart failure (NYHA Class III or IV) in those patients who remain symptomatic despite stable, optimal medical therapy, and have a left ventricular ejection fraction d35% and a prolonged QRS duration
FDA Enforcement
Class II
·Terminated·St Jude Medical Inc.·October 25, 2017