24 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MICROSCOPE KNOB COVER, STERILE, DISPOSABLE
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
NA
FDA UDI
Stryker Leibinger GmbH & Co. KG·07613327370706·FACIAL ID-RECON-1PLATE
Zavation
FDA UDI
Zavation LLC·00197157001964·Modular Screwdriver
Zavation
FDA UDI
Zavation LLC·00197157001957·Modular Screwdriver
Zavation
FDA UDI
Zavation LLC·00197157001933·Modular Screwdriver
Zavation
FDA UDI
Zavation LLC·00197157001940·Modular Screwdriver
PENLIGHT/SWAB HOLDER
FDA 510(k)
FDA Class 1
·General Hospital
MYRIAN 1.4
FDA 510(k)
FDA Class 2
·Radiology
ABC
FDA UDI
Conmed Corporation·20653405986284·ABC WIRELESS FOOTSWITCH
Persona®
FDA UDI
Zimmer, Inc.·00889024557765·
Persona®
FDA UDI
Zimmer, Inc.·00889024557987·
Persona®
FDA UDI
Zimmer, Inc.·00889024558083·
Persona®
FDA UDI
Zimmer, Inc.·00889024560192·
Persona®
FDA UDI
Zimmer, Inc.·00889024558038·
Persona®
FDA UDI
Zimmer, Inc.·00889024560413·
SCREWDRIVER SHAFT, COMPRESSION T2 TIBIA 3.5 MM
FDA Adverse Event
Malfunction
·STRYKER OSTEOSYNTHESIS KIEL·Product code HXX·July 27, 2012
LEAD MODEL 302
FDA Adverse Event
Malfunction
·CYBERONICS, INC.·Product code LYJ·October 29, 2010
DURATA STS OPTIM PASSIVE FIXATION LEAD
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL INC., CARDIAC RHYTHM MANAGEMENT D·Product code LWS·January 13, 2014
GENESYS HTA PROCERVA®
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MARLBOROUGH·Product code MNB·December 31, 2012
INSTRUMENT, ULTRASONIC SURGICAL
FDA Adverse Event
Injury
·ETHICON ENDO-SURGERY, LLC.·Product code LFL·March 30, 2026