10,000 results · 59ms · Sources: EU EUDAMED, 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