10,000 results
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59ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MICRO/MINI N-PK(H) BONE ANCHOR
FDA 510(k)
FDA Class 2
·Orthopedic
MICRO/MINI N-PK(F) BONE ANCHOR
FDA 510(k)
FDA Class 2
·Orthopedic
Hydrafacial Syndeo
FDA UDI
Hydrafacial LLC·00810007532523·100–120VAC, 50/60Hz, 2A
Hydrafacial Syndeo
FDA UDI
Hydrafacial LLC·00810007532516·220-240VAC, 50/60Hz, 2A
Hydrafacial Syndeo
FDA UDI
Hydrafacial LLC·00810007532493·220-240VAC, 50/60Hz, 2A
Hydrafacial Syndeo
FDA UDI
Hydrafacial LLC·00810007532509·HYDRAFACIAL SYNDEO 120V, WHITE (NO PERK)
MEMBRAGEL
FDA Adverse Event
Injury
·INSTITUT STRAUMANN AG·Product code NPK·January 6, 2012
MEMBRAGEL
FDA Adverse Event
Injury
·INSTITUT STRAUMANN AG·Product code NPK·January 6, 2012
MEMBRAGEL
FDA Adverse Event
Injury
·INSTITUT STRAUMANN AG·Product code NPK·January 6, 2012
MEMBRAGEL
FDA Adverse Event
Injury
·INSTITUT STRAUMANN AG·Product code NPK·January 6, 2012
MEMBRAGEL
FDA Adverse Event
Injury
·BIORA AB·Product code NPK·June 21, 2010
MEMBRAGEL
FDA Adverse Event
Injury
·BIORA AB·Product code NPK·April 16, 2010
GUIDOR BIORESORBABLE MATRIX BARRIER
FDA Adverse Event
Injury
·SUNSTAR AMERICAS, INC.·Product code NPK·November 25, 2014
MEMBRAGEL
FDA Adverse Event
Injury
·INSTITUT STRAUMANN AG·Product code NPK·May 23, 2012
BIO-GIDE MEMBRANE (30-8013)
FDA Adverse Event
Injury
·GEISTLICH PHARMA AG·Product code NPK·March 13, 2012
MEMBRANE
FDA Adverse Event
Injury
·INTEGRA LIFE SCIENCES·Product code NPK·April 24, 1996
MEMBRAGEL
FDA Adverse Event
Injury
·BIORA AB·Product code NPK·November 19, 2010
MEMBRGEL
FDA Adverse Event
Injury
·BIORA AB·Product code NPK·October 19, 2010
GORE-TEX REGENERATIVE MEMBRANE-TITANIUM REINFORCED
FDA Adverse Event
Injury
·W.L. GORE & ASSOCIATES,INC·Product code NPK·October 19, 2009
MEMBRAGEL
FDA Adverse Event
Injury
·BIORA AB·Product code NPK·November 19, 2010