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

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DEPUY MOTECH MOSS-MIAMI SPINAL SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

PRESTIGE® LP Cervical Disc System

FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00613994490254·GUIDE 6972568 CUTTER

Cervage

FDA 510(k)
FDA Class 2 ·Orthopedic

MODIFICATION TO OASYS SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

GLIDESCOPE COBALT AVL BATON 3-4

FDA Adverse Event
Malfunction ·VERATHON MEDICAL (CANADA) ULC.·Product code CCW·February 15, 2013

ORTHO SUMMIT SAMPLE HANDLING SYSTEM

FDA Adverse Event
Malfunction ·HAMILTON BONADUZ AG·Product code JQW·January 28, 2011

SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

FDA Adverse Event
Injury ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·August 1, 2014

NSK

FDA Adverse Event
Injury ·NAKANISHI INC.·Product code EGS·April 26, 2018

NSK

FDA Adverse Event
Injury ·NAKANISHI, INC.·Product code EGS·May 12, 2015

Disposable Light Handle Cover, Item Number B1-715-65. Packaged 1 device inside a peel pouch and sealed. Sealed pouches are packaged 10 each inside a poly liner. 5 rows of 10 pouches are placed in a labeled corrugated mailer box. Product Usage: Intended to be used as a disposable barrier for a surgical lighting system and which allows a surgical team member to manually adjust the lighting system. Single use device.

FDA Recall
Terminated ·Ecolab, Inc.·Product code FTA·October 13, 2017

NSK

FDA Adverse Event
Malfunction ·NAKANISHI INC.·Product code EGS·October 9, 2025

NSK

FDA Adverse Event
Injury ·NAKANISHI INC.·Product code EGS·December 19, 2016

NSK

FDA Adverse Event
Injury ·NAKANISHI INC.·Product code EGS·March 1, 2018

NSK

FDA Adverse Event
Injury ·NAKANISHI INC.·Product code EGS·January 15, 2018

NSK

FDA Adverse Event
Injury ·NAKANISHI INC.·Product code EGS·June 6, 2018

DA-800C5L

FDA Adverse Event
Injury ·NAKANISHI INC.·Product code EGS·May 2, 2016

NSK

FDA Adverse Event
Injury ·NAKANISHI INC.·Product code EGS·April 26, 2018

DA-400CIII

FDA Adverse Event
Injury ·NAKANISHI INC. (NSK)·Product code EGS·May 26, 2015