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

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

MSI 9000 SERIES BED

FDA 510(k)
FDA Class 2 ·General Hospital

6440 Ultrasound System

FDA 510(k)
FDA Class 2 ·Radiology

CAPSTONE SPINAL SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

CAPSTONE SPINAL SYSTEM

FDA Adverse Event
Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code MAX·November 29, 2019

CAPSTONE VERTEBRAL BODY SPACER

FDA Adverse Event
Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code MAX·July 3, 2017

CD HORIZON® SPINAL SYSTEM

FDA Adverse Event
Injury ·MDT PUERTO RICO OPERATIONS CO, MED REL·Product code KWP·November 14, 2018

FILLER, RECOMBINANT HUMAN BONE MORPHOGENETIC P

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NEK·January 22, 2020

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·February 22, 2021

CAPSTONE CAGE

FDA Adverse Event
Injury ·MEDTRONIC·Product code MAX·November 19, 2015

CAPSTONE SPINAL SYSTEM

FDA Adverse Event
Malfunction ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code MAX·October 26, 2018

CAPSTONE VERTEBRAL BODY SPACER

FDA Adverse Event
Malfunction ·WARSAW ORTHOPEDIC INC.·Product code MAX·July 2, 2009

CAPSTONE SYSTEM

FDA Adverse Event
Malfunction ·SOFAMOR DANEK DEGGENDORF GMBH·Product code MQP·September 3, 2010

CAPSTONE® SPINAL SYSTEM

FDA Adverse Event
Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code MAX·April 17, 2014

CAPSTONE SPINAL SYSTEM

FDA Adverse Event
Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code MAX·October 18, 2017

CAPSTONE SPINAL SYSTEM

FDA Adverse Event
Malfunction ·WARSAW ORTHOPEDIC INC.·Product code MAX·December 21, 2009

HOMECHOICE AUTOMATED PD SET WITH CASSETTE

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·June 13, 2014

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·December 13, 2012

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 27, 2015

CAPSTONE SPINAL SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK·Product code MAX·October 10, 2014

CAPSTONE SYSTEM

FDA Adverse Event
Malfunction ·SOFAMOR DANEK DEGGENDORF GMBH·Product code MAX·November 4, 2010