9 results
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29ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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MedCAD® AccuPlan® System
FDA 510(k)
FDA Class 2
·Dental
CoRoent
FDA UDI
Nuvasive, Inc.·00887517639400·CoRoent Ant TLIF PEEK, 9x12x28mm 12°
STERILISATION TRAY XL
FDA UDI
Aktormed GmbH·04260463842821·autoclavable accessories for the DEXTER ENDOSCO...
M VISUM ALERT ALARM MANAGEMENT SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
THE VARIA FIBULA LOCKED PLATING SYSTEM LINE EXTENSION ADDITION OF STRAIGHT PLATES
FDA 510(k)
FDA Class 2
·Orthopedic
FG SAFELIGHT FIBER OPTIC CABLE WITH ADVANCED IMAGING MODALITY RIGHT ANGLE 5 MM
FDA Adverse Event
Malfunction
·STRYKER ENDOSCOPY-SAN JOSE·Product code OWN·March 5, 2025
LIGAMAX 5MM
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code FZP·October 22, 2014
UNKNOWN M2A MAGNUM HIP
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·June 27, 2013
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN INC.·Product code NBW·August 4, 2011