27 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Embrella Endoscopic Distal Attachment
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
ATLANTIS® Anterior Cervical Plate System
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00763000868062·PLATE 6190030 ANTERIOR CERVICAL 30MM
ATLANTIS® Anterior Cervical Plate System
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00613994235824·PLATE 6190030 ANTERIOR CERVICAL 30MM
Greenwald Surgical Company, Inc.
FDA UDI
GRACE MANUFACTURING, INC.·10801334008932·Otis Bougie-a-Boule. Mirror finish, stainless s...
OsteoMed
FDA UDI
OSTEOMED LLC·00845694041003·3.0mm x 0 Degree ExtremiFuse Implant
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690189701·AK3 Patella Medial Hole Drill Guide
Stimulator, Bone Growth, Non-Invasive
FDA Pre-Market Approval
FDA Class 2
·ActaStim-S Spine Fusion Stimulator
OsteoMed
FDA UDI
OSTEOMED LLC·00845694069960·ExtremiFuse 3.0mm 0 Degree Implant Sterile Qty 5
NA
FDA UDI
STRYKER CORPORATION·04546540373212·6.0mm Acorn
NA
FDA UDI
STRYKER CORPORATION·04546540373229·7.5mm Acorn
NA
FDA UDI
STRYKER CORPORATION·04546540373236·9.0mm Acorn
EXPECT ENDOSCOPIC ASPIRATION NEEDLE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
TAPERLOC COMPLETE SIZE 4MM AND XR 123
FDA 510(k)
FDA Class 2
·Orthopedic
Stimulator, Bone Growth, Non-Invasive
FDA Pre-Market Approval
FDA Class 2
·ActaStim-S Spine Fusion Stimulator
Stimulator, Bone Growth, Non-Invasive
FDA Pre-Market Approval
FDA Class 2
·ActaStim-S Non Invasive Spine Fusion Stimulator
Stimulator, Bone Growth, Non-Invasive
FDA Pre-Market Approval
FDA Class 2
·ActaStim-S Spine Fusion Stimulator
Stimulator, Bone Growth, Non-Invasive
FDA Pre-Market Approval
FDA Class 2
·ActaStim-S
7900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·June 18, 2013
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 4, 2011
HEARTSTART FRX
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·September 18, 2014