24 results
·
23ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
MODIFICATION TO AUTOFUSER
FDA 510(k)
FDA Class 2
·General Hospital
LEONE SPA
FDA UDI
LEONE SPA·08033707065654·INTRAORAL ELASTICS 2,5 oz 1/4" red
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690189404·AK3 Femoral Distal Locating Device, Fixed Bushing
JOBST Elvarex
FDA UDI
BSN-Jobst GmbH·04019702356922·Elvarex 2/Knee High/Slant-Open Toe/Dotted 2,5 c...
NIDO Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07315K0103000·Caddie, Domino Connectors
JOBST Elvarex
FDA UDI
BSN-Jobst GmbH·04019702501384·Elvarex 3/Knee High/Slant-Open Toe-Elephantiasi...
MEDTRONIC MODEL 7495LZ LOW IMPEDANCE EXTENSION
FDA 510(k)
FDA Class 2
·Neurology
LIGHTSPEED 2.0CT SCANNER SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code KWP·November 15, 2013
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·MDT SOFAMOR DANEK USA, INC.·Product code KWP·October 30, 2019
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·June 26, 2020
CD HORIZON® SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·April 30, 2018
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·January 14, 2020
CD HORIZON® SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·April 30, 2018
HOMECHOICE AUTOMATED PD SET WITH CASSETTE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·May 2, 2013
STRATA® II VALVE, SMALL
FDA Adverse Event
Malfunction
·MEDTRONIC NEUROSURGERY·Product code JXG·September 15, 2014
HOMECHOICE LOW RECIRCULATION VOLUME APD SET WITH CASSETTE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·May 16, 2011
CONFIDENCE KIT, NO NEEDLES
FDA Adverse Event
Malfunction
·DEPUY SYNTHES SPINE·Product code NDN·April 1, 2014
CD HORIZON® SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·May 8, 2017
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code KWP·February 2, 2021