19 results · 19ms · 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

TREATMENT RECLINER

FDA Adverse Event
Malfunction ·STRYKER MEDICAL·Product code FRK·February 3, 2011

8010042-2008-00010

FDA Adverse Event
Malfunction ·Product code CBK·January 25, 2008