1,514 results
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21ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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ODC INDUSTRIES
FDA registration
ODC INDUSTRIES·1 product·🇫🇷 France
ODC
FDA UDI
Howmedica Osteonics Corp.·07613327032581·Acetabular Cup
ODC
FDA UDI
Howmedica Osteonics Corp.·07613327039177·Acetabular Cup
ODC
FDA UDI
Howmedica Osteonics Corp.·07613327039184·Acetabular Cup
ODC
FDA UDI
Howmedica Osteonics Corp.·07613327032598·Acetabular Cup
ScleralEase
FDA UDI
ODC INDUSTRIES·03770020907586·All-in-One Scleral Lens Application and Removal...
ScleralEase
FDA UDI
ODC INDUSTRIES·03770020907593·All-in-One Scleral Lens Application and Removal...
ODC B2 BIPOLAR CUP
FDA 510(k)
FDA Class 2
·Orthopedic
OMNIFIT/OMNIFLEX/ODC/OMNIFIT-HA HIP STEM SERIES
FDA 510(k)
FDA Class 2
·Orthopedic
UNICEL® DXC 800 PRO SYNCHRON® CHEMISTRY ANALYZER
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code JJE·July 15, 2011
VENUS DIAMOND PLT REFILL 1x10x0,25G ODC
FDA UDI
Kulzer GmbH·J014660467330·Dental Composite resin
VENUS DIAMOND SYRINGE REFILL 1x4G ODC
FDA UDI
Kulzer GmbH·J014660467370·Dental Composite resin
UNICEL DXC 800 SYNCHRON SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code JJE·March 26, 2012
SYNCHRON CX DELTA CLINICAL SYSTEM, MODEL CX5
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code JJE·November 18, 2011
SYNCHRON CX9 ALX
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code JJE·October 14, 2010
HEX DRIVER; 2.5MM
FDA Adverse Event
Malfunction
·INTEGRA LIFESCIENCES CORPORATION OH/USA·Product code HXX·March 9, 2015
HEX DRIVER, 2.5MM
FDA Adverse Event
Malfunction
·INTEGRA LIFESCIENCES CORPORATION OH/USA·Product code HXX·March 9, 2015
SYNCHON CX DELTA CLINICAL SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code JJE·December 7, 2011
OSTEONICS ODC HIP STEM
FDA Adverse Event
Injury
·HOWMEDICA OSTEONICS·Product code KWY·October 1, 2001
SYNCHRON® LX20 PRO CLINICAL SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code JJE·August 18, 2011