25 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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DIGITAL ULTRASONIC DIAGNOSTIC IMAGING SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B16741318300·
Ophthalmic Spatula
FDA UDI
KATENA PRODUCTS, INC.·00841668102213·ENDOTHELIAL STRIPPER
Meridian
FDA UDI
Seaspine Orthopedics Corporation·10889981265892·Trial, 39mm x 30mm x 18mm, 30 Deg
Meridian
FDA UDI
Seaspine Orthopedics Corporation·10889981246648·Interbody, 39mm x 30mm X 18mm, 30 Deg
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B1674131830060·
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B167311318300·
TALOS® HA PEEK IBF
FDA UDI
MEDITECH SPINE, LLC·B167321318300·
SAFEPRO PLUS SAFETY SYRINGE
FDA 510(k)
FDA Class 2
·General Hospital
ZMACHINE, MODEL DT-100
FDA 510(k)
FDA Class 2
·Neurology
ACCU-CHEK ® MULTICLIX
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code FMK·October 1, 2014
CORDLESS DRIVER 3
FDA Adverse Event
Malfunction
·STRYKER INSTRUMENTS-KALAMAZOO·Product code HRX·May 29, 2013
TREK CORONARY DILATATION CATHETER
FDA Adverse Event
Malfunction
·AV-TEMECULA-CT·Product code LOX·June 16, 2011
UNKNOWN OXFORD BEARING
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JWH·February 16, 2018
UNKNOWN OXFORD FEMORAL COMPONENT
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code HRY·February 16, 2018
UNKNOWN OXFORD BEARING
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code HRY·February 16, 2018
UNKNOWN OXFORD TIBIAL COMPONENT
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JWH·February 16, 2018
UNKNOWN OXFORD FEMORAL COMPONENT
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JWH·February 16, 2018
UNKNOWN OXFORD BEARING
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JWH·February 16, 2018
UNKNOWN OXFORD BEARING
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JWH·February 16, 2018