25 results · 21ms · Sources: EU EUDAMED, US FDA

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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