239 results
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29ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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INMODE WMFACE DEVICE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B16711409260·
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587P1409260·14mm PLIF Implant 9mm Wide 26mm Length
Gyrus ACMI
FDA UDI
Gyrus ACMI, LLC·00821925014367·JAHN HYDROXYLVENT TUBE 1.27 MM ID 9.5 MM LENGTH...
ZEUS-P
FDA UDI
SPINAL ELEMENTS·00840916153403·Zeus-P Trial, 14 x 9 x 26mm
Ardis®
FDA UDI
ZIMMER SPINE, INC.·00889024334649·
Ardis®
FDA UDI
ZIMMER SPINE, INC.·00889024333918·
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587P14092670·14mm PLIF Implant 9mm Wide 26mm Length 7 Degrees
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B1671001409260·
ARROWHEAD FIXATION DEVICE
FDA 510(k)
FDA Class 2
·Orthopedic
ULTRASOUND SCANNER, HUDSON MODELS 8000 AND 9000
FDA 510(k)
FDA Class 2
·Radiology
GMK-SPHERE 02.07.1204R TIBIAL TRAY FIXED CEMENTED SIZE 4 R
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·August 2, 2023
GMK-SPHERE TIBIAL TRAY FIXED CEMENTED SIZE 5
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·April 29, 2019
GMK SPHERE IMPLANTS
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·November 4, 2025
FREESTYLE LITE
FDA Adverse Event
Malfunction
·Product code NBW·June 3, 2013
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS, INC.·Product code JAA·September 3, 2008
OPTIFLUX 160NRE DIALYZER
FDA Adverse Event
Injury
·OGDEN MANUFACTURING·Product code FJI·June 21, 2011
GMK-SPHERE 02.07.1206L TIBIAL TRAY FIXED CEMENTED SIZE 6 L
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·April 20, 2022
GMK-SPHERE FEMORAL COMPONENT SPHERE CEMENTED SIZE 5 R
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·November 22, 2021
GMK-SPHERE TIBIAL TRAY FIXED CEMENTED SIZE T3-I4 L
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·January 30, 2019