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

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PreludeSYNC DISTAL Radial Compression System

FDA 510(k)
FDA Class 2 ·Cardiovascular

RESTORIS

FDA UDI
MAKO SURGICAL CORP.·00848486001636·MCK Inlay Tibial Component

RESTORIS

FDA UDI
MAKO SURGICAL CORP.·00848486001087·MCK Inlay Tibial Component

RESTORIS

FDA UDI
MAKO SURGICAL CORP.·00848486001063·MCK Inlay Tibial Component

RESTORIS

FDA UDI
MAKO SURGICAL CORP.·00848486001629·MCK Inlay Tibial Component

RESTORIS

FDA UDI
MAKO SURGICAL CORP.·00848486001605·MCK Inlay Tibial Component

RESTORIS

FDA UDI
MAKO SURGICAL CORP.·00848486001612·MCK Inlay Tibial Component

RESTORIS

FDA UDI
MAKO SURGICAL CORP.·00848486001643·MCK Inlay Tibial Component

RESTORIS

FDA UDI
MAKO SURGICAL CORP.·00848486001650·MCK Inlay Tibial Component

RESTORIS

FDA UDI
MAKO SURGICAL CORP.·00848486001070·MCK Inlay Tibial Component

SignaLoc Screw

FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215116743·

OLYMPUS EMPOWER H65

FDA Adverse Event
Malfunction ·QUANTA SYSTEM S.P.A.·Product code GEX·May 19, 2022

SRI LP GOWN

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

DISPOSABLE CIRCULAR STAPLER, DISPOSABLE CIRCULAR STAPLER MODEL KYGW-25.5, KYGW-28.5

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

BD¿ SYRINGE WITH NEEDLE

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code FMF·October 30, 2018

PIPELINE

FDA Adverse Event
Malfunction ·MICRO THERAPEUTICS, INC. DBA EV3·Product code OUT·March 17, 2020

POWERED WHEELCHAIR

FDA Adverse Event
Malfunction ·INVACARE TAYLOR STREET·Product code ITI·June 20, 2013

PED FLTR W/CLV

FDA Adverse Event
Malfunction ·HOSPIRA, LTD.·Product code FPA·May 5, 2011

3003135857-2008-00045

FDA Adverse Event
Malfunction ·Product code CBK·July 21, 2008

EXPRESSEW III AC+ GUN

FDA Adverse Event
Malfunction ·MEDOS INTERNATIONAL SARL·Product code LXH·February 1, 2022