28 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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DELTA HUMERAL CUPS
FDA 510(k)
FDA Class 2
·Orthopedic
NVM5
FDA UDI
Nuvasive, Inc.·00887517207272·NVM5 Needle Module, SSEP
PULSE
FDA UDI
Nuvasive, Inc.·00195377051547·PULSE Hip Pin Kit, 15cm
EndoAVF® Balloon Inflation Kit
FDA UDI
Merit Medical Systems, Inc.·00884450413838·
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450469880·
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450480045·
InTess Lumbar Cage
FDA UDI
Kalitec Direct LLC·B07312K0103150·Shaver, Closed, 15mm
neoWave LS
FDA UDI
XENIX MEDICAL LLC·00818345024106·Paddle Shaver, 15mm
VENTRICULAR ANALYSIS TOOLKIT OPTION
FDA 510(k)
FDA Class 2
·Radiology
ISCREEN VISION SCREENER
FDA 510(k)
FDA Class 2
·Ophthalmic
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·March 3, 2025
AEQ REV II GLENOID BASEPLATE DIA 25MM
FDA Adverse Event
Injury
·TORNIER S.A.S.·Product code PHX·July 1, 2025
AEQUALIS REVERSED BASE PLATE TA6V LONG PEG WITH HA
FDA Adverse Event
Injury
·TORNIER S.A.S.·Product code KWS·March 13, 2025
AEQ REV GLENOID BASEPLATE 29MM
FDA Adverse Event
Injury
·TORNIER S.A.S.·Product code KWS·March 6, 2025
HEARTSTREAM FR2
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·March 14, 2013
TECNIS
FDA Adverse Event
Injury
·ADVANCED MEDICAL OPTICS·Product code HQL·May 22, 2008
CONTAK RENEWAL
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code NIK·April 12, 2011
AEQUALIS REVERSED MULTIDIRECTIONAL GLENOID PLATE HA
FDA Adverse Event
Injury
·TORNIER S.A.S.·Product code KWS·March 25, 2024
D.4,5MM COMPRESSION SCREW L.32MM
FDA Adverse Event
Injury
·TORNIER S.A.S.·Product code KWS·January 7, 2025
D.4,5MM COMPRESSION SCREW L.23MM
FDA Adverse Event
Injury
·TORNIER S.A.S.·Product code KWS·January 7, 2025