26 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Faros Mobile
FDA 510(k)
FDA Class 2
·Cardiovascular
N/A
FDA UDI
Intersurgical Incorporated·05030267140848·22mm Smoothbore breathing system with monitorin...
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X1820300·18mm H x 20mm W x 30mm L x 0 degrees XLIF
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B16741820300·
FX V 135 stem
FDA UDI
FX SOLUTIONS·03701037318515·FX V135 LONG STEM TA6V CEMENTLESS Ø40/14 LG200m...
OsteoMed
FDA UDI
OSTEOMED LLC·00842528127476·2.0 X 30mm Cannulated Headed Screw, T7
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X18203080·18mm H x 20mm W x 30mm L x 8 degrees XLIF
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587L182030120·18mm H x 20mm W x 30mm L XLIF Trial 12 degree L...
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X182030120·18mm H x 20mm W x 30mm L x 12 degrees XLIF
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B1674182030060·
DIMENSION VISTA CSAE CALIBRATOR, MODEL KC440
FDA 510(k)
FDA Class 2
·Clinical Toxicology
SYNTHES RADIAL HEAD PROSTHESIS SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
PROSTHESIS, ELBOW, HEMI-RADIAL, POLYMER
FDA Adverse Event
Malfunction
·SYNTHES MONUMENT·Product code KWI·January 25, 2017
M2A-MAGNUM TAPER INSERT
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·March 10, 2017
COLLEAGUE CX VOLUMETRIC INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·October 2, 2008
XENFORM
FDA Adverse Event
Other
·TEI BIOSCIENCES INC.·Product code FTM·June 17, 2013
LIFEPAK 1000 DEFIBRILLATOR
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC.·Product code MKJ·June 22, 2011
8MM TI STRAIGHT RADIAL STEM 28MM-STERILE
FDA Adverse Event
Injury
·SYNTHES MONUMENT·Product code KWI·January 24, 2017
22MM COCR RADIAL HEAD STANDARD HEIGHT/12.5MM-STERILE
FDA Adverse Event
Injury
·SYNTHES MONUMENT·Product code KWI·January 24, 2017
18MM COCR RADIAL HEAD STANDARD HEIGHT/11.5MM-STERILE
FDA Adverse Event
Injury
·SYNTHES MONUMENT·Product code KWI·September 7, 2017