31 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ULTRASONIC SCALER
FDA 510(k)
FDA Class 2
·Dental
NSK
FDA Adverse Event
Injury
·NAKANISHI INC.·Product code ELC·April 29, 2020
NSK
FDA Adverse Event
Malfunction
·NAKANISHI INC.·Product code ELC·May 31, 2023
Oticon
FDA UDI
Oticon A/S·05707131234865·K50,ITCP PB DIR L BE KIT
Marienfeld Superior
FDA UDI
Paul Marienfeld GmbH & Co. KG·04250317337375·
Fixion Nailing System
FDA UDI
CARBOFIX ORTHOPEDICS LTD·07290109330204·The nail is intended for use in the fixation of...
N/A
FDA UDI
HANS RUDOLPH, INC.·00874750003303·65 V2 LARGE 22ID ELBOW W/HG
Plateau Spacer System
FDA UDI
Life Spine, Inc.·00190837045289·Large Spacer Caddy
ABX PENTRA CREATININE 120 CP; ABX PENTRA MULTICAL; ABX PENTRA N CONTROL; ABX PENTRA P CONTROL; ABX PENTRA URINE CONTROL
FDA 510(k)
FDA Class 2
·Clinical Chemistry
SPIRODOC
FDA 510(k)
FDA Class 2
·Anesthesiology
HAHN TAPERED IMPLANT Ø4.3 X 8 MM
FDA Adverse Event
Injury
·PRISMATIK DENTALCRAFT, INC.·Product code DZE·September 4, 2024
HAHN TAPERED IMPLANT Ø4.3 X 8 MM
FDA Adverse Event
Injury
·PRISMATIK DENTALCRAFT, INC.·Product code DZE·August 15, 2023
HAHN TAPERED IMPLANT Ø4.3 X 8 MM
FDA Adverse Event
Injury
·PRISMATIK DENTALCRAFT, INC.·Product code DZE·June 17, 2023
EVOLUTION® COLONIC CONTROLLED-RELEASE STENT - UNCOVERED
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code MQR·April 12, 2018
HAHN TAPERED IMPLANT Ø4.3 X 8 MM
FDA Adverse Event
Injury
·PRISMATIK DENTALCRAFT, INC.·Product code DZE·October 11, 2023
STEALTHSTATION TRIA NAVIGATION SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC NAVIGATION, INC.·Product code HAW·May 15, 2013
POWERED WHEELCHAIR
FDA Adverse Event
Malfunction
·INVACARE TAYLOR STREET·Product code ITI·September 24, 2014
SM104 M-SERIES W/5TH WHEEL
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FPO·May 24, 2011
EVOLUTION® COLONIC CONTROLLED-RELEASE STENT - UNCOVERED
FDA Adverse Event
Injury
·COOK IRELAND LTD·Product code MQR·August 17, 2017
EVOLUTION BILIARY CONTROLLED-RELEASE STENT - FULLY COVERED
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FAD·March 12, 2015