7 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Arthrex Mini Comprehensive Fixation System - 1.0mm Screws
FDA 510(k)
FDA Class 2
·Orthopedic
V.A.C. VERAFLO CLEANSE DRESSING SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
PRUCLAIR NONSTEROIDAL CREAM
FDA 510(k)
FDA Unclassified
·Unknown
LAP-BAND AP ADJUSTABLE GASTRIC BANDING SYSTEM (SMALL) ACCESS PORT I
FDA Adverse Event
Malfunction
·COSTA RICA·Product code LTI·October 6, 2008
MINIMAGNUM KNOTLESS IMPLANT
FDA Adverse Event
Malfunction
·ARTHROCARE CORPORATION·Product code HWC·June 25, 2013
EON MINI 16-CHANNEL RECHARGEABLE IPG
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·July 21, 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