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

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8000229

FDA Adverse Event
Malfunction ·LASER PERIPHERALS, LLC·Product code GEX·August 7, 2025

8000229

FDA Adverse Event
Malfunction ·LASER PERIPHERALS, LLC·Product code GEX·August 7, 2025

8000229

FDA Adverse Event
Malfunction ·LASER PERIPHERALS, LLC·Product code GEX·August 7, 2025

8000229

FDA Adverse Event
Malfunction ·LASER PERIPHERALS, LLC·Product code GEX·August 7, 2025

8000229

FDA Adverse Event
Malfunction ·LASER PERIPHERALS, LLC·Product code GEX·January 24, 2023

8000229

FDA Adverse Event
Malfunction ·LASER PERIPHERALS, LLC·Product code GEX·June 16, 2023

8000229

FDA Adverse Event
Malfunction ·LASER PERIPHERALS, LLC·Product code GEX·May 7, 2025

LUMIRADX SARS-COV-2 AG TEST STRIP KIT

FDA Adverse Event
Malfunction ·LUMIRADX UK LTD.·Product code QKP·February 25, 2021

LUMIRADX SARS-COV-2 AG TEST STRIP KIT

FDA Adverse Event
Malfunction ·LUMIRADX UK LTD.·Product code QKP·February 25, 2021

LUMIRADX SARS-COV-2 AG TEST STRIP KIT

FDA Adverse Event
Malfunction ·LUMIRADX UK LTD.·Product code QKP·February 25, 2021

LUMIRADX SARS-COV-2 AG TEST STRIP KIT

FDA Adverse Event
Malfunction ·LUMIRADX UK LTD.·Product code QKP·February 25, 2021

LUMIRADX SARS-COV-2 AG TEST STRIP KIT

FDA Adverse Event
Malfunction ·LUMIRADX UK LTD.·Product code QKP·February 25, 2021

LUMIRADX SARS-COV-2 AG TEST STRIP KIT

FDA Adverse Event
Malfunction ·LUMIRADX UK LTD.·Product code QKP·February 25, 2021

LUMIRADX SARS-COV-2 AG TEST STRIP KIT

FDA Adverse Event
Malfunction ·LUMIRADX UK LTD.·Product code QKP·February 25, 2021

LUMIRADX SARS-COV-2 AG TEST STRIP KIT

FDA Adverse Event
Malfunction ·LUMIRADX UK LTD.·Product code QKP·February 25, 2021

LUMIRADX SARS-COV-2 AG TEST STRIP KIT

FDA Adverse Event
Malfunction ·LUMIRADX UK LTD.·Product code QKP·February 25, 2021

LUMIRADX SARS-COV-2 AG TEST STRIP KIT

FDA Adverse Event
Malfunction ·LUMIRADX UK LTD.·Product code QKP·February 25, 2021

POLYFORM SYNTHETIC MESH

FDA Adverse Event
Injury ·PROXY BIOMEDICAL LTD.·Product code FTL·November 22, 2012

LOGIC FEMORAL PS CEM LEFT SZ 2

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·December 31, 2024

LOGIC TIBIA PS MOD INSRT SZ 2 9MM

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·August 23, 2024