14 results
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24ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04049772814299·GENUMEDI PT SILVER R VI
Visionaire Disposable Instruments
FDA 510(k)
FDA Class 2
·Orthopedic
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04049772814237·GENUMEDI PT SILVER L VI
MSI Precision Specialty Instruments
FDA UDI
Med Saver, Inc.·00194613097851·Vienna Nasal Speculum, Number 1, 30mm Modified ...
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587A143226120·14mm H x 32mm W x 26mm L x 12 degrees ALIF
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587A14322680·14mm H x 32mm W x 26mm L x 8 degrees ALIF
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587A143226150·14mm H x 32mm W x 26mm L x 15 degrees ALIF
ENDURE IMPLANT, MODELS 3508, 4308, 3520, 4320
FDA 510(k)
FDA Class 2
·Dental
STERILIZATION MATS
FDA 510(k)
FDA Class 2
·General Hospital
GMK-SPHERE TIBIAL INSERT FIXED SPHERE FLEX SIZE 3/11 MM R
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·May 17, 2021
BD PRECISIONGLIDE NEEDLE
FDA Adverse Event
Malfunction
·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FMI·March 7, 2021
NOVATION
FDA Adverse Event
Other
·EXACTECH INC·Product code KXD·May 28, 2013
EON MINI
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·September 22, 2014
75MM SELECTABLE NEW TLC
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code GDW·June 28, 2011