110 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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INDIKO
FDA 510(k)
FDA Class 1
·Clinical Chemistry
Sapphire 1100 35
FDA UDI
SIZEWISE RENTALS, L.L.C.·00845699000951·120V Sapphire 1100 35 Rev 1 and Rev 2
OsteoMed
FDA UDI
OSTEOMED LLC·00845694040068·PrimaLIF 5mm Kerrison Rongeur, Forward
LEONE SPA
FDA UDI
LEONE SPA·08033707096948·BKT 35 INTERACTIVE SL 22 T-22 BH
CORTICAL BONE SCREW 3.5mm x 35mm
FDA UDI
ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665034110·
Cosmolock
FDA UDI
Kalitec Direct LLC·B07311K1100530·Caddie, 7.5mm Screws
MODEL VISULAS 532S LASER WITH THE VITE OPTION
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
IVS TUNNELLER
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
CORTICAL BONE SCREW, Ø3.5MM X 35MM
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code HSB·October 3, 2022
WAVEWRITER ALPHA
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·July 14, 2023
Stent, Iliac
FDA Pre-Market Approval
FDA Class 3
·EPIC SELF-EXPANDING NITINOL STENT SYSTEM
PARADIGM INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code LZG·May 13, 2013
PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code MGB·September 23, 2014
GREENLIGHT ADDSTAT
FDA Adverse Event
Malfunction
·AMS, INNOVATION CENTER - SILICON VALLEY·Product code GEX·May 17, 2011
Stent, Iliac
FDA Pre-Market Approval
FDA Class 3
·EPIC VASCULAR SELF-EXPANDING STENT SYSTEM
Stent, Iliac
FDA Pre-Market Approval
FDA Class 3
·EPIC VASCULAR SELF EXPANDING STENT SYSTEM
Stent, Iliac
FDA Pre-Market Approval
FDA Class 3
·EPIC VASCULAR SELF-EXPANDING STENT SYSTEM
Stent, Iliac
FDA Pre-Market Approval
FDA Class 3
·Epic Vascular Self-Expanding Stent System
Stent, Iliac
FDA Pre-Market Approval
FDA Class 3
·EPIC SELF-EXPANDING NITINOL STENT SYSTEM
Stent, Iliac
FDA Pre-Market Approval
FDA Class 3
·Epic Self Expanding Stent System