25 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SYNTHES (USA) MEDIUM EXTERNAL FIXATION SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04051526780828·LEVAMED ACTIVE ANKLE SUP SLVR R IV
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04051526189799·LEVAMED ACTIVE ANKLE SUP BLACK R IV
Endo Carry-on Procedure Kit
FDA UDI
MEDIVATORS INC.·00677964153167·Endo Carry-on Procedure Kit contains Basin, VIA...
Cosmolock
FDA UDI
Kalitec Direct LLC·B07311K0112340·Tap, 6.50mm, Fixed Sleeve
QUICK SET
FDA Adverse Event
Injury
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·November 28, 2025
IntuBrite Sterile
FDA UDI
SALTER LABS·00607411966309·Miller 4 SINGLE USE DISPOSABLE LARYNGOSCOPE BL...
QUICK-SET
FDA Adverse Event
Injury
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·August 8, 2025
QUICK SET
FDA Adverse Event
Injury
·UNOMEDICAL A/S·Product code FPA·October 30, 2025
QUICK-SET
FDA Adverse Event
Injury
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·August 7, 2025
QUICK SET
FDA Adverse Event
Injury
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·September 18, 2025
QUICK SET
FDA Adverse Event
Injury
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·August 21, 2025
DOUBLE LUMEN URETHANE PICC LINE, MODEL UPICDS-
FDA 510(k)
FDA Class 2
·General Hospital
MODEL APS ALTERNANS PROCESSING SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
QUICK SET
FDA Adverse Event
Malfunction
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·September 24, 2025
SHOULDER SYSTEM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code PHX·February 14, 2025
CURE CATHETER
FDA Adverse Event
Injury
·CURE MEDICAL LLC·Product code EZD·October 7, 2021
AXON PATIENT MODULE
FDA Adverse Event
Malfunction
·MEDTRONIC XOMED, INC.·Product code GWF·March 14, 2013
PRECISION XTRA
FDA Adverse Event
Malfunction
·Product code NBW·March 8, 2011
PARAGON
FDA Adverse Event
Malfunction
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DXY·March 10, 2008