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

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SAGEMAX Z-BLANK

FDA 510(k)
FDA Class 2 ·Dental

VANGUARD REPROCESSED ARTHROSCOPIC WANDS

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

MEMODYN STAPLE

FDA 510(k)
FDA Class 2 ·Orthopedic

ENTERPRISE VASCULAR RECONSTRUCTION DEVICE AND DELIVERY SYSTEM

FDA Adverse Event
Injury ·CORDIS NEUROVASCULAR, INC.·Product code NJE·April 17, 2013

VERSACARE

FDA Adverse Event
Malfunction ·HILL-ROM RITTER·Product code FNL·June 18, 2008

PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

FDA Adverse Event
Injury ·MEDTRONIC MINIMED·Product code MDS·April 12, 2011

TRIO LX SMALL CONNECTOR

FDA Adverse Event
Malfunction ·STRYKER SPINE BORDEAUX·Product code MNI·March 23, 2011

Smiths Medical CADD" Yellow Medication Cassette Reservoir with flow stop, clamp and female Luer. Non-vented stopper included 100mL, Product Code 21-7300-24

FDA Enforcement
Class II ·Ongoing·ICU Medical Inc.·September 10, 2025

ENDOTAK RELIANCE

FDA Adverse Event
Malfunction ·CPI - DEL CARIBE·Product code NVY·July 20, 2011

OT ULTRA METER

FDA Adverse Event
Malfunction ·LIFESCAN INC.·Product code NBW·April 3, 2012

OT ULTRA METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·May 27, 2011

OT ULTRA METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·April 3, 2012

OT ULTRA METER

FDA Adverse Event
Injury ·LIFESCAN, INC.·Product code NBW·October 6, 2010

OT ULTRA METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·June 1, 2011

OT ULTRA METER

FDA Adverse Event
Injury ·LIFESCAN, INC.·Product code NBW·September 16, 2010

OT ULTRA METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·March 19, 2012

OT ULTRA METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·December 22, 2010

OT ULTRA METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·November 30, 2010

OT ULTRA METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·September 2, 2011

OT ULTRA METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·January 12, 2011