21 results
·
36ms
·
Sources: EU EUDAMED, US FDA
TEMP. & GSR BIOFEEDBACK DEVICE
FDA 510(k)
FDA Class 2
·Neurology
LUNA INTERBODY SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
FUJI COMPUTED RADIOGRAPHY (FCR) CLEARVIEW CS IMAGE READER
FDA 510(k)
FDA Class 2
·Radiology
NA
FDA UDI
Zimmer, Inc.·00889024193963·
NA
FDA UDI
Zimmer, Inc.·00889024633681·
NA
FDA UDI
Zimmer, Inc.·00889024633650·
NA
FDA UDI
Zimmer, Inc.·00889024633667·
NA
FDA UDI
Zimmer, Inc.·00889024193987·
NA
FDA UDI
Zimmer, Inc.·00889024193994·
NA
FDA UDI
Zimmer, Inc.·00889024633674·
NA
FDA UDI
Zimmer, Inc.·00889024193970·
NA
FDA UDI
Zimmer, Inc.·00889024633643·
NA
FDA UDI
Zimmer, Inc.·00889024194007·
NA
FDA UDI
Zimmer, Inc.·00889024194014·
NA
FDA UDI
Zimmer, Inc.·00889024633698·
UNKNOWN BONE SCREW
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.1818910·Product code HWC·May 31, 2014
EGR SYSTEM (STERILE)
FDA Adverse Event
Injury
·INTEGRA LIFESCIENCES CORPORATION OH/USA·Product code NBH·November 12, 2012
SOLETRA
FDA Adverse Event
Injury
·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code MHY·September 21, 2010
PDS II POLYDIOXANONE SUTURE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code NEW·April 8, 2024
VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAM·April 8, 2024