10,000 results · 38ms · Sources: EU EUDAMED, US FDA

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CENTRAL BODY F/MEF MAX-L 437 MIN-L 287

FDA Adverse Event
Injury ·SYNTHES HAGENDORF·Product code HST·March 8, 2016

O-RING F/392.901

FDA Adverse Event
Injury ·SYNTHES (USA)·Product code HST·March 8, 2016

O-RING F/392.901

FDA Adverse Event
Injury ·SYNTHES (USA)·Product code HST·March 8, 2016

RADIESSE DERMAL FILLER

FDA Adverse Event
Injury ·BIOFORM MEDICAL·Product code LMH·January 23, 2008

STD-CLAMP F/MEF

FDA Adverse Event
Malfunction ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code KTT·October 12, 2018

STD-CLAMP F/MEF

FDA Adverse Event
Malfunction ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code LXH·November 26, 2018

STD-CLAMP F/MEF

FDA Adverse Event
Malfunction ·SYNTHES GMBH·Product code LXH·June 24, 2013

STD-CLAMP F/MEF

FDA Adverse Event
Malfunction ·SYNTHES GMBH·Product code LXH·June 25, 2013

STD-CLAMP F/MEF

FDA Adverse Event
Malfunction ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code KTT·October 12, 2018

SLEEV 2PART L50 F/MEF

FDA Adverse Event
Malfunction ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code FZX·November 26, 2018

SLEEV 2PART L50 F/MEF

FDA Adverse Event
Malfunction ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code FZX·November 26, 2018

SLEEV 2PART L50 F/MEF

FDA Adverse Event
Malfunction ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code LXH·October 12, 2018

SLEEV 2PART L50 F/MEF

FDA Adverse Event
Malfunction ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code LXH·October 12, 2018

SLEEVE F/SEGM-TRANSP F/MEF

FDA Adverse Event
Malfunction ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code FZX·November 26, 2018

SLEEVE F/SEGM-TRANSP F/MEF

FDA Adverse Event
Malfunction ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code LXH·October 12, 2018

SLEEVE F/SEGM-TRANSP F/MEF

FDA Adverse Event
Injury ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code LXH·February 28, 2019

DRILLSL 7/6 LONG F/MEF

FDA Adverse Event
Malfunction ·SYNTHES GMBH·Product code FZX·June 23, 2025

DRILLSL 7/6 LONG F/MEF

FDA Adverse Event
Malfunction ·SYNTHES GMBH·Product code FZX·June 23, 2025

DRILLSL 7/6 LONG F/MEF

FDA Adverse Event
Malfunction ·SYNTHES GMBH·Product code FZX·June 23, 2025

CARDIAC CATHETER

FDA Adverse Event
Injury ·Product code DRF·February 11, 2016