16 results · 22ms · Sources: EU EUDAMED, US FDA

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SYNTHES LOCKING CALCANEAL PLATES

FDA 510(k)
FDA Class 2 ·Orthopedic

Novalung System

FDA 510(k)
FDA Class 2 ·Cardiovascular

WOMED NICRO-CRAFT POWER SYSTEM

FDA 510(k)
FDA Class 2 ·Ear, Nose, Throat

BD VACUTAINER® CPT¿ NH: ~130 IU FICOLL¿: 2.0ML

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO.·Product code JCF·June 6, 2018

BD VACUTAINER® CPT¿ NH: ~130 IU FICOLL¿: 2.0ML

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO.·Product code JCF·June 7, 2018

BD VACUTAINER® CPT¿ NH: ~130 IU FICOLL¿: 2.0ML

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO.·Product code JCF·June 6, 2018

BD VACUTAINER® CPT¿ NH: ~130 IU FICOLL¿: 2.0ML

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO.·Product code JCF·April 27, 2018

TITANIUM SCREW LOW PROFILE 5X40MM

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code KWT·November 18, 2016

BD VACUTAINER® CPT¿ NH: ~130 IU FICOLL¿: 2.0ML

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO.·Product code JCF·April 16, 2018

TITANIUM SCREW LOW PROFILE 5X40MM

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code KWT·November 18, 2016

IN TOUCH ZU

FDA Adverse Event
Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FNL·March 6, 2013

CAPSURE Z

FDA Adverse Event
Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·February 15, 2011

CAPSUREFIX NOVUS

FDA Adverse Event
Injury ·MPRI·Product code DTB·August 8, 2014

BD VACUTAINER® CPT¿ NH: ~130 IU FICOLL¿: 2.0ML

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO.·Product code JCF·June 5, 2018

Candela Smoothbeam Laser System Model Numbers: 9914-00-0820 9914-06-0820 9914-07-0820 9914-08-0820 9914-10-0820 Units are the same except for color

FDA Recall
Terminated ·Candela Laser Corporation·Product code GEX·November 25, 2003

Philips Zenition 50, Model Number: 718096

FDA Enforcement
Class II ·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·November 20, 2024