15 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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LDV((Low Dead Volume )Syringe
FDA 510(k)
FDA Class 2
·General Hospital
NEXT Fine Bubblegum Prophy Paste Box 200
FDA UDI
Preventech·D024220083·NEXT Fine Bubblegum Prophy Paste Box of 200 2.0...
Corneal Trephine
FDA UDI
KATENA PRODUCTS, INC.·00841668112687·BARRON CORNEAL PUNCH 9.25MM
Sapphire NC Plus
FDA UDI
OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955916519·Percutaneous Transluminal Coronary Angioplasty ...
TriVerse Tibial Offset Cutting Block
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215097400·
TUTA HEALTHCARE ARTHROSCOPY FLUSHING SET, MODEL 80.601
FDA 510(k)
FDA Class 2
·Orthopedic
SET SCREW FOR TI TROCHANTERIC FIXATION NAIL(TFN)
FDA 510(k)
FDA Class 2
·Orthopedic
INDIGO SYSTEM ASPIRATION CATHETER 7D
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code QEW·August 3, 2022
INDIGO SYSTEM ASPIRATION CATHETER 7D
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code QEW·August 20, 2022
ACCU-CHEK COMFORT CURVE TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·October 31, 2008
INRATIO
FDA Adverse Event
Malfunction
·ALERE SAN DIEGO, INC.·Product code GJS·August 12, 2011
FORTIFY VR, DF4 CONNECTOR
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·July 11, 2013
INDIGO SYSTEM SEPARATOR 7D
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code QEW·September 13, 2022
INDIGO SYSTEM ASPIRATION CATHETER 7D
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code QEW·October 13, 2023
Model Number L111, ESSENTIO DR SL MRI Pacemaker
FDA Enforcement
Class I
·Ongoing·Boston Scientific Corporation·October 22, 2025