44 results
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54ms
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Sources: EU EUDAMED, US FDA
LIFE INSTRUMENT CORP.
FDA registration
LIFE INSTRUMENT CORP.·20 products·🇺🇸 United States
Life Instruments Corp
FDA UDI
Life Instrument Corporation·M93071018001CB0·18" Curette #0 Angled, 9" Handle Black Coated
LIFE INSTRUMENT
FDA Adverse Event
Injury
·LIFE INSTRUMENT CORP.·Product code HTX·September 17, 2024
3MM KERRISON RONGEUR
FDA Adverse Event
Injury
·LIFE INSTRUMENT CORP.·Product code HTX·August 2, 2024
KERRISON RONGUER 3MM
FDA Adverse Event
Injury
·LIFE INSTRUMENT CORP.·Product code HTX·April 4, 2022
2MM KERRISON RONGEUR
FDA Adverse Event
Injury
·LIFE INSTRUMENT CORP.·Product code HTX·December 27, 2023
*
FDA Adverse Event
Malfunction
·LIFE INSTRUMENT CORP.·Product code HTX·December 2, 2014
2MM KERRISON RONGEUR
FDA Adverse Event
Injury
·LIFE INSTRUMENT CORP.·Product code HTX·October 9, 2024
KERRISON RONGEUR 4MM
FDA Adverse Event
Injury
·LIFE INSTRUMENT CORP.·Product code HTX·November 13, 2024
LIFE INSTRUMENT CO. 4MM KERRISON RONGEUR
FDA Adverse Event
Injury
·LIFE INSTRUMENT CORP·Product code HAO·December 4, 2024
*
FDA Adverse Event
Malfunction
·LIFE INSTRUMENT CORP·Product code HTX·September 23, 2013
*
FDA Adverse Event
LIFE INSTRUMENT CORP.·Product code HAE·August 28, 2013
MICRO BALL PROBE
FDA Adverse Event
Malfunction
·LIFE INSTRUMENT CORP.·Product code HXB·April 7, 2017
LIFE INSTRUMENT CO CURETTE
FDA Adverse Event
Malfunction
·LIFE INSTRUMENT CORP.·Product code FZS·January 20, 2021
KERRISON RONGEUR
FDA Adverse Event
Malfunction
·LIFE INSTRUMENT CORP.·Product code JXG·May 7, 2018
LIFE INSTRUMENT BLACK HANDLE NERVE HOOK
FDA Adverse Event
Malfunction
·LIFE INSTRUMENT CORP·Product code GDG·July 26, 2019
15 ELECTRODE DBL. INSULATED SPATULA TIP
FDA Adverse Event
Malfunction
·LIFE LINES MEDICAL, INC.( LIFE INSTRUMENT CORP.)·Product code KNF·August 30, 2004
VERITI DX THERMAL CYCLER
FDA Adverse Event
Malfunction
·LIFE TECHNOLOGIES HOLDINGS PTE. LTD.·Product code NSU·March 25, 2014
BELMONT INSTRUMENT CORP
FDA Adverse Event
Injury
·*·Product code LGZ·January 12, 2007
MILLIS OSTEOTOME
FDA Adverse Event
Malfunction
·LIFE INSTRUMENTS CORP.·Product code HWM·April 20, 2011