26 results
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24ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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neon3 universal OCT spinal stabilization
FDA 510(k)
FDA Class 2
·Orthopedic
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B16721610320·
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B1672161032060·
ORTHOPEDIC SALVAGE SYSTEM (OSS)
FDA UDI
Biomet Orthopedics, LLC·00880304250932·
16PW - ACCO
FDA UDI
Certified Safety Manufacturing, Inc.·00766588110325·16PW - ACCO
ZEUS-T
FDA UDI
SPINAL ELEMENTS·00840916124113·Zeus-TLIF Implant, Size 16H x 10W x 32L
CARDO MEDICAL FEMORAL CEMENT RESTRICTOR, MODEL 503-MCRX
FDA 510(k)
FDA Class 2
·Orthopedic
DEPOTONE
FDA 510(k)
FDA Class 2
·General Hospital
CAPSUREFIX NOVUS
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 13, 2010
KYPHON XPEDE BONE CEMENT
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NDN·December 21, 2018
KYPHON XPEDE BONE CEMENT
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NDN·May 29, 2019
KYPHON XPEDE BONE CEMENT
FDA Adverse Event
Malfunction
·MDT KYPHON NEUCHATEL MFG·Product code NDN·February 28, 2019
KYPHON XPEDE BONE CEMENT
FDA Adverse Event
Malfunction
·MDT KYPHON NEUCHATEL MFG·Product code NDN·February 28, 2019
1030489-2019-01511
FDA Adverse Event
Death
·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NDN·December 31, 2019
LOGIC TIBIA PS MOD INSRT SZ 3 9MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·May 7, 2024
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 11, 2013
UNICEL DXC 800 SYNCHRON SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code JJE·June 17, 2011
ATTAIN OTW
FDA Adverse Event
Injury
·MPRI·Product code LWP·October 10, 2014
1030489-2019-01423
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code NDN·December 13, 2019
KYPHX® HV-R¿ BONE CEMENT
FDA Adverse Event
Malfunction
·CARDIAC SURGERY MFG KERKRADE·Product code NDN·September 8, 2021