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

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ACCUFLATE

FDA 510(k)
FDA Class 1 ·General, Plastic Surgery

NuVasive

FDA UDI
Nuvasive, Inc.·00887517390974·CoRoent XLW Trial, 12x22x50mm 10°

N/A

FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00721902930300·INSTRUMENT 8910512 ALIF TRIAL 12MM

ZAVATION

FDA UDI
Zavation LLC·00842166151703·WHITNEY 13mmx15mm , 5deg , 12mm

UCR

FDA UDI
Seaspine Orthopedics Corporation·10889981079994·4MM HEX SHAFT

SmartBand EMR Kit, SmartBand EMR Pack, SmartSnare

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

SIMMETRY SACROILIAC JOINT FUSION SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

ESSURE

FDA Adverse Event
Injury ·BAYER PHARMA AG·Product code HHS·September 27, 2019

OT ULTRA METER

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

ENDOTAK RELIANCE

FDA Adverse Event
Injury ·CPI - DEL CARIBE·Product code LWS·July 2, 2014

R SERIES DEFIBRILLATOR

FDA Adverse Event
Malfunction ·ZOLL MEDICAL CORPORATION, WORLD WIDE HEADQUARTERS·Product code MKJ·November 30, 2012

BD BACTEC¿ MYCO/F LYTIC CULTURE VIALS

FDA Adverse Event
Malfunction ·BECTON DICKINSON CARIBE LTD.·Product code MDB·March 20, 2023

ESSURE

FDA Adverse Event
Injury ·BAYER PHARMA AG·Product code HHS·December 5, 2017

ESSURE

FDA Adverse Event
Injury ·BAYER PHARMA AG·Product code HHS·June 25, 2019

ESSURE

FDA Adverse Event
Injury ·BAYER PHARMA AG·Product code HHS·November 23, 2017

ESSURE

FDA Adverse Event
Injury ·BAYER PHARMA AG·Product code HHS·November 3, 2017

BD BACTEC¿ MYCO/F LYTIC CULTURE VIALS

FDA Adverse Event
Malfunction ·BECTON DICKINSON CARIBE LTD.·Product code MDB·November 4, 2025

BD BACTEC¿ MYCO/F LYTIC CULTURE VIALS

FDA Adverse Event
Malfunction ·BECTON DICKINSON CARIBE LTD.·Product code MDB·January 11, 2023

BD BACTEC¿ MYCO/F LYTIC CULTURE VIALS

FDA Adverse Event
Malfunction ·BECTON DICKINSON CARIBE LTD.·Product code MDB·September 9, 2022

ESSURE

FDA Adverse Event
Injury ·BAYER PHARMA AG·Product code HHS·September 8, 2017