27 results
·
20ms
·
Sources: EU EUDAMED, US FDA
iovera system
FDA 510(k)
FDA Class 2
·Neurology
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B16741618350·
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B1674161835060·
ers2 ECG Receiver
FDA UDI
ergoline GmbH·04059358001753·
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X1618350·16mm H x 18mm W x 35mm L x 0 degrees XLIF
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587L161835120·16mm H x 18mm W x 35mm L XLIF Trial 12 degree L...
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X161835120·16mm H x 18mm W x 35mm L x 12 degrees XLIF
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X16183580·16mm H x 18mm W x 35mm L x 8 degrees XLIF
STRYKER SILVERGLIDE BIPOLAR FORCEPS REUSABLE CABLE; DISPOSABLE CABLE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
MEDPOR FIXATION SYSTEM-CRANIAL, MODELS 80080, 80079
FDA 510(k)
FDA Class 2
·Neurology
AESCULAP SURGICAL INSTRUMENTS
FDA Adverse Event
Injury
·CHRISTOPH MIETHKE GMBH & CO. KG·Product code JXG·November 27, 2019
AESCULAP SURGICAL INSTRUMENTS
FDA Adverse Event
Injury
·CHRISTOPH MIETHKE GMBH & CO. KG·Product code JXG·November 27, 2019
Matrixx System
FDA UDI
NEXXT SPINE, LLC·00889929065969·Corpectomy, 16Dx18Wx35H 0°
Matrixx System
FDA UDI
NEXXT SPINE, LLC·00889929066355·Corpectomy, 16Dx18Wx35H 6°
DRIVER; SIZE 10
FDA Adverse Event
Malfunction
·K2M, INC.·Product code LXH·July 12, 2022
ACRYSERT DELIVERY SYSTEM
FDA Adverse Event
Injury
·ALCON RESEARCH, LTD. / HUNTINGTON·Product code HQL·July 8, 2011
MICRBR GEMSTR 1.2 FLTR PP Y-SITE 96IN
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FRN·June 3, 2013
MAXIMO II DR
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LWS·October 10, 2014
CUP: MPACT DOUBLE MOBILITY ACETABULAR SHELL 52
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LPH·May 6, 2021
MECTACER BIOLOX DELTA FEMORAL BALL HEAD
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LZO·May 7, 2025