8 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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VaPro Plus Pocket, VaPro Plus
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
E-PASS
FDA 510(k)
FDA Class 2
·Cardiovascular
AIDA DIAGNOSTIC ULTRASOUND SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
VSP SYSTEM
FDA Adverse Event
Injury
·3D SYSTEMS·Product code DZJ·December 18, 2020
9-10MM EZLOC FEMORAL FIXATION STD.
FDA Adverse Event
Malfunction
·BIOMET SPORTS MEDICINE·Product code MBI·October 8, 2008
CLARION IMPLANT
FDA Adverse Event
Malfunction
·ADVANCED BIONICS, LLC·Product code MCM·June 25, 2013
CANE, CRUTCH AND WALKER TIPS AND PADS
FDA Adverse Event
UNKNOWN·Product code INP·August 5, 2011
Boston Scientific Fetch 2 Aspiration Catheter, Catalog No. 109400-001. Product The Fetch 2 Aspiration Catheter is indicated for the removal of fresh, soft emboli and thrombi from vessels in the peripheral and coronary vasculature.
FDA Enforcement
Class I
·Terminated·Boston Scientific Corporation·April 27, 2016