15 results · 21ms · Sources: EU EUDAMED, US FDA

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CODAN SAFEFEED ENTERAL FEEDING RESERVOIR

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

n/a

FDA UDI
HANS RUDOLPH, INC.·00874750006236·2384B MINI 2WAY NRBV T-SHAPE

FORCETRIAD ELECTROSURGICAL GENERATOR

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

TRIMAX

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

AWL Ø2 ANGL

FDA Adverse Event
Malfunction ·SYNTHES GMBH·Product code OVE·January 8, 2013

CONTOUR

FDA Adverse Event
Malfunction ·BAYER HEALTHCARE LLC·Product code NBW·March 26, 2013

AWL Ø2 ANGL

FDA Adverse Event
Malfunction ·SYNTHES GMBH·Product code OVE·January 7, 2013

AWL Ø2 ANGL

FDA Adverse Event
Malfunction ·SYNTHES GMBH·Product code OVE·January 7, 2013

CONTOUR USB

FDA Adverse Event
Malfunction ·BAYER HEALTHCARE LLC·Product code NBW·December 14, 2012

CONTOUR NEXT

FDA Adverse Event
Injury ·BAYER HEALTHCARE LLC·Product code NBW·July 27, 2012

GORE EXCLUDER AAA ENDOPROSTHESIS

FDA Adverse Event
Injury ·W. L. GORE & ASSOCIATES·Product code MIH·May 24, 2011

DEPUY ASR XL FEM IMP SIZE 53

FDA Adverse Event
Injury ·DEPUY INTERNATIONAL·Product code KWA·May 14, 2013

PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

FDA Adverse Event
Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·September 23, 2014

19.5 X 86 X 1.27MM (.050 INCH) OSCILLATOR BLADE

FDA Adverse Event
Malfunction ·CONMED CORPORATION·Product code GFA·February 16, 2021

INLIVEN CRT-P, Model Numbers: a) V284 b) V285 c) W274 d) W275 (added 7/15/2021)

FDA Enforcement
Class I ·Ongoing·Boston Scientific Corporation·July 21, 2021