10 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SENSITOUCH
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
9MM CUTTING REAMER
FDA UDI
Biomet Orthopedics, LLC·00880304464360·
Cutting Reamer
FDA UDI
Biomet Orthopedics, LLC·00887868556692·
EMULATE
FDA UDI
BENCO DENTAL SUPPLY CO.·D74439047690·Emulate Advanced Alginate Fast Set Case of 8 Po...
CHALLENGE 6000 POWERED MUSCLE STIMULATOR
FDA 510(k)
FDA Class 2
·Physical Medicine
PERCOR STAT DL 9.5 FR 34CC INTRA-AORTIC BALLOON
FDA 510(k)
FDA Class 2
·Cardiovascular
STEALTHSTATION¿ S8 SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC NAVIGATION, INC.·Product code HAW·November 5, 2025
INFUSE BONE GRAFT
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·January 9, 2013
PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM
FDA Adverse Event
Injury
·AV-REDWOOD CITY·Product code MGB·November 22, 2010
TELIGEN
FDA Adverse Event
Malfunction
·GUIDANT CRM CLONMEL IRELAND·Product code LWP·July 1, 2014