365 results · 23ms · Sources: EU EUDAMED, US FDA

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Lithotriptor, Extracorporeal Shock-Wave, Urological

FDA Pre-Market Approval
FDA Class 2 ·RICHARD WOLF PIEZOLITH E.L.P. LITHOTRIPT MODEL2300

ReLine

FDA UDI
Nuvasive, Inc.·00195377042989·RELINE-C Lockscrew Repeater

Trimline

FDA UDI
ORMCO CORPORATION·00889989052497·LOWER LEFT SECOND MOLAR TRIMLINE BAND SIZE 13

KOTEX SUPER MAXI PADS

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

COLLAMER ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER THREE PIECE

FDA Adverse Event
Malfunction ·STAAR SURGICAL CO.·Product code HQL·June 23, 2006

VerSys®

FDA UDI
Zimmer, Inc.·00889024140226·

VerSys®

FDA UDI
Zimmer, Inc.·00889024140219·

MYCARELINK

FDA Adverse Event
Malfunction ·PLEXUS MANUFACTURING SDN. BHD·Product code NVZ·May 3, 2018

MYCARELINK

FDA Adverse Event
Malfunction ·PLEXUS MANUFACTURING SDN. BHD·Product code NVZ·May 3, 2018

COLLAMER ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER THREE PIECE

FDA Adverse Event
Malfunction ·STAAR SURGICAL CO.·Product code HQL·June 23, 2006

COLLAMER ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER SINGLE PIEC

FDA Adverse Event
Injury ·STAAR SURGICAL CO.·Product code HQL·June 15, 2006

COLLAMER ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER SINGLE PIEC

FDA Adverse Event
Malfunction ·STAAR SURGICAL·Product code HQL·June 15, 2006

COLLAMER ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER THREE PIECE

FDA Adverse Event
Malfunction ·STAAR SURGICAL CO.·Product code HQL·June 23, 2006

COLLAMER ULTRAVIOLET ABSORBING POSTERIOR CHAMBER THREE PIECE

FDA Adverse Event
Injury ·STAAR SURGICAL CO.·Product code HQL·June 15, 2006

COLLAMER ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER THREE PIECE

FDA Adverse Event
Malfunction ·STAAR SURGICAL CO.·Product code HQL·June 23, 2006

COLLAMER ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER THREE PIECE

FDA Adverse Event
Injury ·STAAR SURGICAL CO.·Product code HQL·June 21, 2006

COLLAMER ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER THREE PIEC

FDA Adverse Event
Malfunction ·STAAR SURGICAL CO.·Product code HQL·June 23, 2006

MYCARELINK

FDA Adverse Event
Malfunction ·PLEXUS MANUFACTURING SDN. BHD·Product code NVZ·June 15, 2018

ECHELON LINEAR CUTTER

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·June 24, 2014

CONTAK RENEWAL

FDA Adverse Event
Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·November 3, 2010