24 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SYNERGEYES HYBRID CONTACT LENSES - DAILY WEAR, MODELS A, M, KC AND PS
FDA 510(k)
FDA Class 2
·Ophthalmic
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587T0810340·8mm TLIF Implant 10mm Wide 34mm Length
Cannulated Headless Compression Screw, 1/2 Threaded, 3.5mm x 34mm
FDA UDI
ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665025194·
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587T08103470·8mm TLIF Implant 10mm Wide 34mm Length 7 Degrees
FIX-L PEEK PLIF and T-PLIF System
FDA UDI
Jeil Medical Corporation·08800089472956·
FIX-L PEEK PLIF and T-PLIF System
FDA UDI
Jeil Medical Corporation·08800089472932·
FIX-L PEEK PLIF and T-PLIF System
FDA UDI
Jeil Medical Corporation·08800089472949·
FIX-L PEEK PLIF and T-PLIF System
FDA UDI
Jeil Medical Corporation·08800089472970·
FIX-L PEEK PLIF and T-PLIF System
FDA UDI
Jeil Medical Corporation·08800089472901·
FIX-L PEEK PLIF and T-PLIF System
FDA UDI
Jeil Medical Corporation·08800089472925·
FIX-L PEEK PLIF and T-PLIF System
FDA UDI
Jeil Medical Corporation·08800089472963·
FIX-L PEEK PLIF and T-PLIF System
FDA UDI
Jeil Medical Corporation·08800089472918·
CD197-PE
FDA UDI
Miltenyi Biotec B.V. & Co. KG·04049934134258·REA108 recognizes human CD197 which is a chemok...
MODEL APS ALTERNANS PROCESSING SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
SYNTHES (USA) MEDIUM EXTERNAL FIXATION SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
ATLANTIS® ANTERIOR CERVICAL PLATE SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWQ·July 12, 2017
ATLANTIS ANTERIOR CERVICAL PLATE SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWQ·May 2, 2017
UNKNOWN_NEUROVASCULAR_PRODUCT
FDA Adverse Event
Injury
·CONCENTRIC MEDICAL·Product code NRY·December 14, 2012
PULSE GEN MODEL 102
FDA Adverse Event
Death
·CYBERONICS INC·Product code LYJ·April 26, 2013
7900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·April 14, 2011