14 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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DOMED TRI-PEG PATELLA, HIGHLY CROSS LINKED DOMED TRI-PEG PATELLA WITH VE
FDA 510(k)
FDA Class 2
·Orthopedic
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B16741218350·
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B1674121835060·
EXIN
FDA UDI
FOREMOUNT ENTERPRISE CO., LTD.·04719871893517·Standard cushion mask with valve #5
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X1218350·12mm H x 18mm W x 35mm L x 0 degrees XLIF
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587L121835120·12mm H x 18mm W x 35mm L XLIF Trial 12 degree L...
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X121835120·12mm H x 18mm W x 35mm L x 12 degrees XLIF
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X12183580·12mm H x 18mm W x 35mm L x 8 degrees XLIF
MEDPOR FIXATION SYSTEM-CRANIAL, MODELS 80080, 80079
FDA 510(k)
FDA Class 2
·Neurology
BRENNEN MEDICAL SURGICAL MESH, GLUCAMESH/GLUCATEX
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
DRIVER; SIZE 10
FDA Adverse Event
Malfunction
·K2M, INC.·Product code LXH·July 12, 2022
WAVELIGHT EX500 EXCIMER LASER
FDA Adverse Event
Injury
·WAVELIGHT GMBH·Product code LZS·May 15, 2013
LASIK
FDA Adverse Event
Injury
·Product code LZS·September 22, 2014
SPRINT FIDELIS
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code LWS·June 13, 2011