90 results · 54ms · Sources: EU EUDAMED, US FDA

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SNOWDEN-PENCER, INC.

FDA Adverse Event
Injury ·SNOWDEN-PENCER·Product code GCJ·January 9, 1998

SNOWDEN PENCER

FDA Adverse Event
Other ·CAREFUSION 2200, INC.·Product code GEI·March 29, 2024

STEVENS TENOTOMY SCS CVD 4-1/2

FDA Adverse Event
Malfunction ·SNOWDEN PENCER, INC.·Product code LRW·January 14, 2004

RETRACTOR, 80MM ANG TRIANGULAR

FDA Adverse Event
Malfunction ·SNOWDEN PENCER, INC.·Product code GAD·January 14, 2004

EMORY RESPOSABLE DISS CVD

FDA Adverse Event
Other ·SNOWDEN PENCER, INC.·Product code GEI·January 20, 2004

RET, TEBBETTS F/O 90MM X 30MM

FDA Adverse Event
Other ·SNOWDEN PENCER, INC.·Product code GAD·February 10, 2004

SWITCH-BLD CURV SCS TIPS CE

FDA Adverse Event
Malfunction ·SNOWDEN PENCER INC.·Product code LRW·January 21, 2004

EMORY RESPOSABLE DISS CVD

FDA Adverse Event
Other ·SNOWDEN PENCER, INC.·Product code GEI·January 2, 2004

SW-BLADE HOOK NEW

FDA Adverse Event
Malfunction ·SNOWDEN PENCER, INC.·Product code LRW·March 4, 2004

STEVENS TENOTOMY SCS CVD 4-1/2

FDA Adverse Event
Malfunction ·SNOWDEN PENCER, INC.·Product code LRW·January 13, 2004

SNOWDEN PENCER

FDA Adverse Event
Other ·SNOWDEN PENCER, INC.·Product code LRW·February 18, 2004

CROW INSUL FCPS 9", 4000 JAW

FDA Adverse Event
Malfunction ·SNOWDEN PENCER, INC.·Product code GEI·March 15, 2002

NO-SCALPEL VAS GRASPING FCP

FDA Adverse Event
Other ·SNOWDEN PENCER, INC.·Product code GEN·March 4, 2002

REUSE SCISSOR SHAFT,INS,5/32

FDA Adverse Event
Malfunction ·SNOWDEN PENCER, INC.·Product code GEI·March 14, 2002

LIGHT SOURCE, PSX 300

FDA Adverse Event
Injury ·SNOWDEN PENCER, INC.·Product code FCW·February 13, 2002

SWITCH-BLADES SCISSOR TIPS

FDA Adverse Event
Malfunction ·SNOWDEN PENCER, INC.·Product code KNS·November 10, 2003

D-L CROCODILE GRASPER RH 5/32

FDA Adverse Event
Malfunction ·SNOWDEN PENCER, INC.·Product code EOQ·October 15, 2003

SWITCH-BLADES SCISSORS TIPS

FDA Adverse Event
Other ·SNOWDEN PENCER, INC.·Product code KNS·November 20, 2003

SNOWDEN PENCER HOOK ELECTRODE

FDA Adverse Event
Malfunction ·SNOWDEN-PENCER INC.·Product code GEI·October 17, 2003

RETRACTOR, 80MM ANG TRIANGULAR

FDA Adverse Event
Malfunction ·SNOWDEN PENCER, INC.·Product code GAD·November 3, 2003