83 results
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20ms
·
Sources: EU EUDAMED, US FDA
RETCAM 3 OPTHALMIC IMAGING SYSTEM
FDA 510(k)
FDA Class 2
·Ophthalmic
GE
FDA UDI
Philips Ds North America LLC·00884838080928·SIGNA 3 0T 8 CH HI RES BRAIN COIL
NU-SPEC D
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
SSW-STERILE SOLUTION WARMER
FDA 510(k)
FDA Class 1
·Physical Medicine
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970010·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172973257·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172973677·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172973301·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970041·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970065·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970027·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970034·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970058·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172973004·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172974018·UniTip High Resolution Catheter 10F
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Injury
·ANIMAS CORPORATION·Product code LZG·May 9, 2013
ARCHITECT I2000SR ANALYZER
FDA Adverse Event
Injury
·ABBOTT MANUFACTURING INC·Product code JJE·September 19, 2014
TRAJECTORY GUIDE KIT, BIOPSY, EXTERNAL
FDA Adverse Event
Malfunction
·MEDTRONIC NAVIGATION, INC.·Product code HAW·April 12, 2011
Allura Xper FD10C; Model Number: 722001; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979, K162859, K161563;
FDA Recall
Open, Classified
·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands·Product code OWB·September 3, 2025
Allura Xper CV20; Model Numbers: 722031; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979, K162859, K161563;
FDA Recall
Open, Classified
·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands·Product code OWB·September 3, 2025