25 results · 22ms · Sources: EU EUDAMED, US FDA

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SONATHERM 600I ULTRASONIC LESION GENERATING SYSTEM

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

APEXPRO TELEMETRY SYSTEM

FDA 510(k)
FDA Class 2 ·Cardiovascular

MODIFICATION TO:LAPAROSCOPIC/ENDOSCOPIC INSTRUMENT

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

PROXIMATE RELOADABLE LINEAR CUTTER WITH SAFETY LOCK-OUT

FDA Adverse Event
Injury ·ETHICON ENDO-SURGERY, INC.·Product code GAG·March 22, 2006

ENDOPATH ETS45 ENDOSCOPIC LINEAR CUTTER - 3.5MM

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code KOG·June 16, 2006

ENDOPATH ETS FLEX45 ENDOSCOPIC ARTICULATING LINEAR

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, INC. (CINCINNATI)·Product code GDW·June 13, 2006

ENDOPATH ETS FLEX45 ENDOSCOPIC ARTICULATING LINEAR

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, INC.(CINCINNATI)·Product code GCJ·June 8, 2006

ENDOPATH ETS FLEX45 ENDOSCOPIC ARTICULATING LINEAR

FDA Adverse Event
Malfunction ·ETHICON ENDO SURGERY, INC. (CINCINNATI)·Product code GCJ·June 19, 2006

ENDOPATH ETS FLEX45 ENDOSCOPIC ARTICULATING LINEAR CUTTER

FDA Adverse Event
Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code GCJ·June 8, 2006

45MM ARTICING LNR CUTR/BLUE RLD

FDA Adverse Event
Injury ·ETHICON ENDO-SURGERY, INC.·Product code GCJ·December 21, 2005

ENDO LINEAR CUTTERS-ETS45MM

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, INC.(CINCINNATI)·Product code KOG·June 8, 2006

ENDOPATH ETS-FLEX45 ARTICULATING ENDOSCOPIC LINEAR

FDA Adverse Event
Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code GDW·June 15, 2006

ENDOPATH ETS45 ENDOSCOPIC LINEAR CUTTER - 2.5 MM -

FDA Adverse Event
Injury ·ETHICON ENDO-SURGERY, INC.(CINCINNATI)·Product code KOG·October 21, 2005

ETS 45 ENDO LINEAR CUTTER BL

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, INC.(CINCINNATI)·Product code KOG·December 19, 2005

NV GXL LINR, NTRL, 32MM ID, GROUP 2 CUPS

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code MEH·July 20, 2022

V40 FEM HEAD ORTHINOX 28+4

FDA Adverse Event
Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code JDI·April 22, 2013

ANIMAS INSULIN INFUSION PUMP

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·April 14, 2011

2600

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·July 9, 2008

NV GXL LNR, LIPPED, 36MM ID, GROUP 3 CUPS

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JDI·July 9, 2024

ENDOPATH ETS FLEX45 ENDOSCOPIC ARTICULATING LINEAR CUTTER

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, INC.(CINCINNATI)·Product code GDW·June 8, 2006