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

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STINGRAY BIPOLAR FORCEPS

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

GEN4 Direct Access

FDA UDI
CURBELL MEDICAL PRODUCTS, INC.·00840828146227·GEN4 Direct Access

INBODY AP1 BODY COMPOSITION ANALYZER

FDA 510(k)
FDA Class 2 ·Cardiovascular

SINGLE USE BILIARY DRAINAGE STENT V

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

UNKNOWN_NEUROVASCULAR_PRODUCT

FDA Adverse Event
Death ·CONCENTRIC MEDICAL·Product code NRY·December 13, 2012

UNKNOWN_NEUROVASCULAR_PRODUCT

FDA Adverse Event
Death ·CONCENTRIC MEDICAL·Product code NRY·December 13, 2012

UNKNOWN_NEUROVASCULAR_PRODUCT

FDA Adverse Event
Death ·CONCENTRIC MEDICAL·Product code NRY·December 13, 2012

MELODY TRANSCATHER PULMONARY

FDA Adverse Event
Injury ·HEART VALVES SANTA ANA·Product code NPV·May 22, 2013

PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

FDA Adverse Event
Injury ·AV-TEMECULA-CT·Product code MGB·September 26, 2014

PRECISE SDS SELF EXPANDING

FDA Adverse Event
Injury ·CORDIS DE MEXICO·Product code FGE·June 14, 2011

UNKNOWN_NEUROVASCULAR_PRODUCT

FDA Adverse Event
Death ·CONCENTRIC MEDICAL·Product code NRY·December 13, 2012

UNKNOWN_NEUROVASCULAR_PRODUCT

FDA Adverse Event
Death ·CONCENTRIC MEDICAL·Product code NRY·December 18, 2012

MEDTRONIC NAVIGATION

FDA Adverse Event
Injury ·MEDTRONIC NAVIGATION, INC·Product code HAW·April 3, 2025

O-ARM IMAGING SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC NAVIGATION, INC (LITTLETON)·Product code OXO·April 3, 2025

BD ULTRA-FINE¿ MINI PEN NEEDLE

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code FMI·January 5, 2022

MAZOR X SYSTEM

FDA Adverse Event
Injury ·MAZOR ROBOTICS LTD·Product code OLO·April 2, 2025