1,677 results · 27ms · Sources: EU EUDAMED, US FDA

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THANH HOA MEDICAL TECHNOLOGY CO., LTD.

FDA registration
THANH HOA MEDICAL TECHNOLOGY CO., LTD.·4 products·🇻🇳 Vietnam

ACTLIFE TECHNOLOGY CO., LTD - THANH HOA BRANCH

FDA registration
ACTLIFE TECHNOLOGY CO., LTD - THANH HOA BRANCH·12 products·🇻🇳 Vietnam

ARROW

FDA UDI
TELEFLEX INCORPORATED·10801902214802·Arterial Catheterization Kit

ARROW

FDA UDI
TELEFLEX INCORPORATED·10801902221350·QuickFlash(R) Radial Artery Catheterization Kit

LASIK

FDA Adverse Event
Injury ·Product code LZS·May 6, 2008

ACRYSOF IQ VIVITY EXTENDED VISION UV ABSORBING IOL

FDA Adverse Event
Injury ·ALCON RESEARCH, LLC - HUNTINGTON·Product code POE·May 11, 2023

WAVELIGHT EX500 LASER

FDA Adverse Event
Injury ·ALCON LABORATORIES, INC.·Product code LZS·December 27, 2023

ALLEGRETTO WAVE EYE-Q

FDA Adverse Event
Injury ·WAVELIGHT AG (PRESSATH)·Product code LZS·July 23, 2010

TECNIS IOL

FDA Adverse Event
Injury ·AMO PUERTO RICO MFG. INC.·Product code HQL·March 4, 2024

PROSTHESIS INTERVERTEBRAL DISC

FDA Adverse Event
Injury ·SYNTHES BRANDYWINE·Product code MJO·May 13, 2015

TECNIS SYMFONY

FDA Adverse Event
Injury ·JOHNSON AND JOHNSON SURGICAL VISION, INC.·Product code POE·July 24, 2018

TECNIS SYMFONY

FDA Adverse Event
Injury ·JOHNSON AND JOHNSON SURGICAL VISION, INC.·Product code POE·July 24, 2018

LASIK EYE (LASER) MACHINE

FDA Adverse Event
Injury ·UNK·Product code LZS·June 15, 2021

ACRYSOF IQ VIVITY TORIC EXTENDED VISION UV ABSORBING IOL

FDA Adverse Event
Injury ·ALCON RESEARCH, LLC - HUNTINGTON·Product code POE·October 28, 2021

UNK

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code HWC·February 22, 2026

UNK

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code HWC·February 22, 2026

LIGHT ADJUSTABLE LENS (LAL)

FDA Adverse Event
Injury ·RXSIGHT, INC.·Product code PZK·February 6, 2024

LASIK

FDA Adverse Event
Injury ·UNKNOWN·Product code LZS·May 23, 2024

DRIVE DEVILBISS HEALTHCARE TITAN AXS K0823 MWD

FDA Adverse Event
Injury ·WU'S TECH (VIETNAM) CO.LTD·Product code ITI·October 22, 2025

UNKNOWN CUP

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDI·July 25, 2024