15 results
·
24ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
SSPC NXT Delivery Catheter
FDA 510(k)
FDA Class 2
·Cardiovascular
XLIF
FDA UDI
Nuvasive, Inc.·00887517199102·MaXcess 4 Blade, 180mm Electrode Ctr
Ophthalmic Cannula
FDA UDI
KATENA PRODUCTS, INC.·00841668114087·SIMCOE CORTEX EXTRACTOR (PK/10)
TAPERLOC COMPLETE RASP/PROVISIONAL
FDA UDI
Biomet Orthopedics, LLC·00880304632516·
STRYKER SPINE TRIO PS
FDA 510(k)
FDA Class 2
·Orthopedic
F3
FDA 510(k)
FDA Class 2
·Physical Medicine
CD HORIZON SOLERA 5.5/6.0
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code HXX·October 21, 2025
ACCU-CHEK ULTRAFLEX INFUSION SET
FDA Adverse Event
Malfunction
·DISETRONIC MEDICAL SYSTEMS·Product code FPA·November 7, 2008
E SERIES DEFIBRILLATOR
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·August 31, 2011
H/S CATHETER SET 7 FRENCH
FDA Adverse Event
Malfunction
·COOPERSURGICAL, INC.·Product code GEH·July 18, 2013
MICRA AV
FDA Adverse Event
Malfunction
·MEDTRONIC IRELAND·Product code PNJ·September 21, 2020
MICRA
FDA Adverse Event
Malfunction
·MEDTRONIC IRELAND·Product code PNJ·July 3, 2020
MICRA
FDA Adverse Event
Malfunction
·MEDTRONIC IRELAND·Product code PNJ·September 9, 2020
HEARTWARE VENTRICULAR ASSIST SYSTEM - CONTROLLER 2.0
FDA Adverse Event
Malfunction
·HEARTWARE, INC.·Product code DSQ·August 31, 2018
MICRA
FDA Adverse Event
Malfunction
·MEDTRONIC IRELAND·Product code PNJ·September 3, 2020