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

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KARL STORZ PUNCTURE, INJECTION, ENDOSCOPIC, VERESS NEEDLE

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

APEX Knee System

FDA UDI
Omni Life Science, Inc.·00841690192343·Apex Revision Knee Reamer - Zimmer 19mm

NYSTAGMOGRAPH EOG/ENG ANALYSES

FDA 510(k)
FDA Class 2 ·Neurology

XENFORM SOFT TISSUE REPAIR MATRIX

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 8, 2013

MODULAR HEAD COMPONENT 28MM HEAD DIAMETER

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code KWA·January 6, 2011

SELUTE PICOTIP

FDA Adverse Event
Injury ·CPI - DEL CARIBE·Product code DTB·July 22, 2014

PENTAX

FDA Adverse Event
Malfunction ·Product code CAL·July 21, 2021

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOQ·February 16, 2022

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOB·October 18, 2021

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOB·October 22, 2021

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOQ·October 22, 2021

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOB·October 22, 2021

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FGB·November 30, 2021

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOB·November 7, 2021

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOB·December 17, 2021

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOQ·July 31, 2021

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOB·February 22, 2022

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOB·September 6, 2023

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOB·April 11, 2022