18 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: 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