25 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
MICRA INTRODUCER SHEATH WITH HYDROPHILIC COATING
FDA 510(k)
FDA Class 2
·Cardiovascular
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B16741320300·
ELMED INCORPORATED
FDA UDI
ELMED INCORPORATED·00198506072949·SINGLEY FORCEPS, 12" (30.5CM)
Meridian
FDA UDI
Seaspine Orthopedics Corporation·10889981265939·Trial, 39mm x 30mm x 20mm, 30 deg
Meridian
FDA UDI
Seaspine Orthopedics Corporation·10889981246686·Interbody, 39mm x 30mm X 20mm, 30 Deg
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B1674132030060·
TALOS° HA PEEK IBF
FDA UDI
MEDITECH SPINE, LLC·B167321320300·
BLINK CL LUBRICANT EYE DROPS
FDA 510(k)
FDA Class 2
·Ophthalmic
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
Arthrex®
FDA UDI
ARTHREX, INC.·00888867412019·Trochanteric nail, 13mm x 20cm x 130°
132030-EMS GENERATOR SYSTEM
FDA Adverse Event
Injury
·DAVOL, INC.(RI)·Product code GEI·June 3, 2002
132030-EMS GENERATOR SYSTEM 5000
FDA Adverse Event
Injury
·DAVOL, INC. (RI)·Product code GEI·March 6, 2003
132030-EMS GENERATOR SYSTEM 5000
FDA Adverse Event
Injury
·DAVOL, INC. (RI)·Product code GEI·August 23, 2001
530G INSULIN PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code OZO·October 1, 2014
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 29, 2013
ASKU
FDA Adverse Event
Malfunction
·MEDTRONIC MILACA INC.·Product code DTE·June 16, 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