7,523 results
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33ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Rectangular Carving Block 1.3
FDA UDI
IMPLANTECH ASSOCIATES, INC.·M724BL13OVFNS1·Rectangular Carving Block 1.3, Opaque, Very Firm
Rectangular Carving Block 2.0
FDA UDI
IMPLANTECH ASSOCIATES, INC.·M724BL20OVFNS1·Rectangular Carving Block 2.0, Opaque, Very Firm
Rectangular Carving Block 1.0
FDA UDI
IMPLANTECH ASSOCIATES, INC.·M724BL10OVFNS1·Rectangular Carving Block 1.0, Opaque, Very Firm
ARTHROSCOPE
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK·Product code HRX·November 26, 2013
CEMENT, BONE, VERTEBROPLASTY
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK·Product code NDN·November 26, 2013
CEMENT, BONE, VERTEBROPLASTY
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK·Product code NDN·November 26, 2013
UNKNOWN
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code MNH·October 28, 2021
UNKNOWN
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code MNH·October 28, 2021
UNKNOWN
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NDN·July 11, 2022
ARTHROSCOPE
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code HRX·August 1, 2013
ARTHROSCOPE
FDA Adverse Event
Malfunction
·MDT KYPHON NEUCHATEL MFG·Product code HRX·January 10, 2020
KYPHX® HV-R? BONE CEMENT
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK·Product code NDN·August 1, 2013
CEMENT, BONE, VERTEBROPLASTY
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK·Product code NDN·August 4, 2015
CEMENT, BONE, VERTEBROPLASTY
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code NDN·March 5, 2019
KYPHX HV-R BONE CEMENT
FDA Adverse Event
Malfunction
·MDT KYPHON NEUCHATEL MFG·Product code NDN·May 16, 2017
REMSTAR AUTO
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code BZD·January 5, 2026
KYPHX HV-R BONE CEMENT
FDA Adverse Event
Malfunction
·MDT KYPHON NEUCHATEL MFG·Product code NDN·July 19, 2020
RADIESSE DERMAL FILLER
FDA Adverse Event
Other
·BIOFORM MEDICAL, INC.·Product code LMH·October 9, 2013
KYPHOPAK TRAY
FDA Adverse Event
Malfunction
·MDT KYPHON NEUCHATEL MFG·Product code LXH·July 24, 2020
CD HORIZON® SOLERA® SPINAL SYSTEM
FDA Adverse Event
Injury
·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code NKB·April 11, 2022