32 results · 25ms · Sources: EU EUDAMED, US FDA

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Metacross OTW PTA Balloon Dilatation Catheter

FDA 510(k)
FDA Class 2 ·Cardiovascular

OHICHO3

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·August 30, 2022

OHICHO3

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·March 18, 2026

METACROSS OTW PTA BALLOON DILATATION CATHETER

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·August 19, 2019

OHICHO NEO

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·February 7, 2024

OHICHO3

FDA Adverse Event
Injury ·Product code LIT·December 26, 2019

SHIRANUI EX

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·August 12, 2020

OHICHO3

FDA Adverse Event
Injury ·Product code LIT·July 19, 2019

PTA BALLOON CATHETER(OHICHO3)

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·December 13, 2017

SHIRANUI EX

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·August 14, 2020

SHIRANUI EX

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·September 30, 2020

OHICHO NEO

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·July 31, 2025

SHIRANUI EX

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·May 28, 2020

OHICHO3

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·September 26, 2018

SHIRANUI EX

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·August 7, 2018

OHICHO3

FDA Adverse Event
Injury ·Product code LIT·September 17, 2019

Epredia

FDA UDI
RICHARD-ALLAN SCIENTIFIC COMPANY·00673693063784·The blades and knifes consumables are for use w...

LACTOSORB® 1.5MM SYSTEM

FDA UDI
BIOMET MICROFIXATION, INC·00841036054311·

Staple Sizer - Red

FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215165246·

MATRYX INTERFERENCE SCREW

FDA 510(k)
FDA Class 2 ·Orthopedic