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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