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