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A. Titan Instruments

FDA UDI
A. TITAN INSTRUMENTS, INC.·00841685111021·Bone Expander Kit, 5 Color Coded Bone Expanders...

BIOTIS ANAEROBIC KBE AGAR

FDA 510(k)
FDA Class 1 ·Microbiology

EVIS EXERA GASTROINTESTINAL VIDEOSCOPE

FDA Adverse Event
Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FDS·December 1, 2020

COLONOVIDEOSCOPE

FDA Adverse Event
Malfunction ·AIZU OLYMPUS CO., LTD.·Product code FDF·January 7, 2026

PROTIME MICROCOAGULATION SYSTEM

FDA Adverse Event
Malfunction ·INTERNATIONAL TECHNIDYNE CORP.·Product code GKP·June 8, 2010

ECHO

FDA Adverse Event
Malfunction ·IMMUCOR·Product code KSZ·March 3, 2009

COLONOVIDEOSCOPE

FDA Adverse Event
Malfunction ·AIZU OLYMPUS CO., LTD.·Product code FDF·October 16, 2024

EVIS EXERA III COLONOVIDEOSCOPE

FDA Adverse Event
Malfunction ·AIZU OLYMPUS CO., LTD.·Product code FDF·April 24, 2025

MW5062882

FDA Adverse Event
Injury ·June 13, 2016

OSSEOSPEED EV 3.6 S - 15 MM

FDA Adverse Event
Injury ·DENTSPLY IMPLANTS MANUFACTURING GMBH·Product code DZE·January 11, 2024

NASAL FORCEPS

FDA Adverse Event
Malfunction ·RICHARD WOLF GMBH·Product code KBE·January 20, 2012

1423537-1997-00104

FDA Adverse Event
Malfunction ·Product code KBE·July 2, 1997

CARRIER WIRE FOR KRAUSE NASAL SNARE

FDA Adverse Event
Malfunction ·ALLEGIANCE/MUELLER·Product code KBE·June 26, 1997

NASAL SNARE WIRE

FDA Adverse Event
Malfunction ·KARL AUGUST HUBER GMBH·Product code KBE·December 24, 2002

PICCOLO XPRESS CHEMISTRY ANALYZER

FDA Adverse Event
Malfunction ·ABAXIS, INC.·Product code JJG·July 22, 2021

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·July 21, 2016

ULTRASONIC GASTROVIDEOSCOPE

FDA Adverse Event
Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code ODG·June 17, 2022

PICCOLO XPRESS CHEMISTRY ANALYZER

FDA Adverse Event
Malfunction ·ABAXIS, INC.·Product code JJG·July 23, 2021

EVIS EXERA II ULTRASONIC BRONCHOFIBERVIDEOSCOPE

FDA Adverse Event
Malfunction ·SHIRAKAWA OLYMPUS CO., LTD.·Product code PSV·April 26, 2023

EVIS EXERA II BRONCHOVIDEOSCOPE

FDA Adverse Event
Malfunction ·AIZU OLYMPUS CO., LTD.·Product code EOQ·April 21, 2023