14 results · 40ms · Sources: EU EUDAMED, US FDA

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STORZ SLX-F2 STORM TOUCH

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

TEMPO AQUA ANGIOGRAPHIC CATHETER

FDA 510(k)
FDA Class 2 ·Cardiovascular

STENT SUPPORT GUIDE CATHETER

FDA 510(k)
FDA Class 2 ·Cardiovascular

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

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

PRECISION NOVI

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·March 16, 2021

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

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

TENSION FREE VAGINAL TAPE

FDA Adverse Event
Injury ·ETHICON, INC.·Product code OTN·April 22, 2013

DEROYAL 1500CC CANISTER KIT, 2 ELBOWS

FDA Adverse Event
Malfunction ·DEROYAL INDUSTRIES, INC.·Product code DWD·April 13, 2011

PROXIMATE PPH PROCEDURE SET

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, LLC·Product code GDW·July 2, 2008

NV GXL LINR, NTRL, 28MM ID, GROUP 1 CUPS

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JDI·October 11, 2024

3.5MM TI CANCELLOUS POLYAXIAL SCREW 22MM

FDA Adverse Event
Injury ·SYNTHES PRODUKTIONS GMBH·Product code NKG·February 8, 2018

NV GXL LINR, NTRL, 36MM ID, GROUP 3 CUPS

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JDI·October 28, 2024

LOCKSCR SYNAPSE TAN

FDA Adverse Event
Injury ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code NKG·February 15, 2018

LOCKSCR SYNAPSE TAN

FDA Adverse Event
Injury ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code NKG·February 15, 2018