31 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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EMIT II PLUS ECSTASY ASSAY
FDA 510(k)
FDA Class 2
·Clinical Toxicology
GEN4 INTERACTIVE
FDA UDI
CURBELL MEDICAL PRODUCTS, INC.·00840828144018·GEN4 INTERACTIVE
NIDO Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07315K0430200·Sagittal Bender, Double Ended Left
NIDO Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07315K0430210·Sagittal Bender, Double Ended Right
PALOMAR SLP 1000
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
CYTOPLAST SUTURE; CS-0318, CS-0416, CS-0418, CS-0513, CS-0513PC, CS-0516HC
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Intelliguides
FDA UDI
Mios Marketing, LLC·G2710430280200·Medial Malleolar Osteotomy Guide, 28mm x 20mm
Intelliguides
FDA UDI
Mios Marketing, LLC·G2710430280220·Medial Malleolar Osteotomy Guide, 28mm x 22mm
Intelliguides
FDA UDI
Mios Marketing, LLC·G2710430280260·Medial Malleolar Osteotomy Guide, 28mm x 26mm
Intelliguides
FDA UDI
Mios Marketing, LLC·G2710430280240·Medial Malleolar Osteotomy Guide, 28mm x 24mm
Intelliguides
FDA UDI
Mios Marketing, LLC·G2710430280300·Medial Malleolar Osteotomy Guide, 28mm x 30mm
Intelliguides
FDA UDI
Mios Marketing, LLC·G2710430280320·Medial Malleolar Osteotomy Guide, 28mm x 32mm
Intelliguides
FDA UDI
Mios Marketing, LLC·G2710430280340·Medial Malleolar Osteotomy Guide, 28mm x 34mm
Intelliguides
FDA UDI
Mios Marketing, LLC·G2710430280280·Medial Malleolar Osteotomy Guide, 28mm x 28mm
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code KWP·November 15, 2013
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK·Product code KWP·November 15, 2013
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code KWP·February 17, 2014
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code KWP·February 17, 2014
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code KWP·February 17, 2014
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code KWP·February 17, 2014