10,000 results
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52ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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LZS
FDA Adverse Event
Injury
·INTRALASE LASER·Product code LZS·August 25, 2008
ANEURX
FDA Adverse Event
Injury
·MEDTRONIC CARDIOVASCULAR·Product code MIH·March 11, 2016
TALENT AAA STENT GRAFT
FDA Adverse Event
Injury
·MEDTRONIC CARDIOVASCULAR·Product code MIH·March 11, 2016
LASIK EXCIMER LASER
FDA Adverse Event
Death
·UNKNOWN·Product code LZS·March 2, 2026
Excimer Laser System
FDA classification
FDA Class 3
·Excimer Laser System
STAR S4 IR Excimer Laser System; Software Version 5.15 Mfg by : AMO Manufacturing USA, LLC 510 Cottonwood Drive Milpitas, CA 95035 Iris registration is designed to compensate for pupil centroid shift and cycloration, both of Which may occur because of patient characteristics and the different environments at the time of measurement and at the time of treatment.
FDA Recall
Terminated
·AMO Manufacturing USA, LLC·Product code LZS·July 18, 2011
Advanced Medical Optics (AMO), VISX WaveScan WaveFront System (software). Part Number 0070-1478. Advanced Medical Optics, Santa Clara, CA 95051.
FDA Recall
Terminated
·Visx Inc·Product code LZS·May 30, 2007
LADARVision Excimer Laser System.
FDA Recall
Terminated
·Alcon Laboratories, Inc.·Product code LZS·August 1, 2005
STAR S4 IR Excimer System (STAR S4 IR) Mfg by AMO Manufacturing USA, LLC 510 Cottonwood Drive Milpitas, CA 95035 The STAR Excimer Laser System, a class Ill device, is indicated for laser assisted in situ keratomileusis (LASIK) eye surgery in certain patient populations.
FDA Recall
Terminated
·Abbott Medical Optics, Inc.·Product code LZS·May 28, 2013
STAR S4 IR Excimer Laser System; Software Version 5.22 Mfg by : AMO Manufacturing USA, LLC 510 Cottonwood Drive Milpitas, CA 95035 Iris registration is designed to compensate for pupil centroid shift and cycloration, both of Which may occur because of patient characteristics and the different environments at the time of measurement and at the time of treatment.
FDA Recall
Terminated
·AMO Manufacturing USA, LLC·Product code LZS·July 18, 2011
STAR S4 IR Excimer Laser System; Software Version 5.21 Mfg by : AMO Manufacturing USA, LLC 510 Cottonwood Drive Milpitas, CA 95035 Iris registration is designed to compensate for pupil centroid shift and cycloration, both of Which may occur because of patient characteristics and the different environments at the time of measurement and at the time of treatment.
FDA Recall
Terminated
·AMO Manufacturing USA, LLC·Product code LZS·July 18, 2011
STAR S4 IR Excimer Laser System; Software Version 5.18 Mfg by : AMO Manufacturing USA, LLC 510 Cottonwood Drive Milpitas, CA 95035 Iris registration is designed to compensate for pupil centroid shift and cycloration, both of Which may occur because of patient characteristics and the different environments at the time of measurement and at the time of treatment.
FDA Recall
Terminated
·AMO Manufacturing USA, LLC·Product code LZS·July 18, 2011
STAR S4 IR Excimer Laser System; Software Version 5.00 Mfg by : AMO Manufacturing USA, LLC 510 Cottonwood Drive Milpitas, CA 95035 Iris registration is designed to compensate for pupil centroid shift and cycloration, both of Which may occur because of patient characteristics and the different environments at the time of measurement and at the time of treatment.
FDA Recall
Terminated
·AMO Manufacturing USA, LLC·Product code LZS·July 18, 2011
STAR S4 IR Excimer Laser System; Software Version 5.16 Mfg by : AMO Manufacturing USA, LLC 510 Cottonwood Drive Milpitas, CA 95035 Iris registration is designed to compensate for pupil centroid shift and cycloration, both of Which may occur because of patient characteristics and the different environments at the time of measurement and at the time of treatment.
FDA Recall
Terminated
·AMO Manufacturing USA, LLC·Product code LZS·July 18, 2011
STAR S4 with Variable Spot Scanning Excimer System (STAR S4) Mfg by AMO Manufacturing USA, LLC 510 Cottonwood Drive Milpitas, CA 95035 The STAR Excimer Laser System, a class Ill device, is indicated for laser assisted in situ keratomileusis (LASIK) eye surgery in certain patient populations.
FDA Recall
Terminated
·Abbott Medical Optics, Inc.·Product code LZS·May 28, 2013
Final Fit Software Version 1.11 and 1.12; PC Based software installed outside Nidek EC-5000 Excimer Laser System. Ophthalmic laser system use for correction of corneal refraction and ablation of the corneal surface. The system is composed of a laser generator which produces an excimer laser radiation of wavelength 193nm, a beam delivery unit, an optical system for observation, a gas system and a computer for system control.
FDA Recall
Terminated
·Nidek Inc·Product code LZS·February 1, 2017
STAR S4 IR Excimer Laser System; Software Version 5.01 Mfg by : AMO Manufacturing USA, LLC 510 Cottonwood Drive Milpitas, CA 95035 Iris registration is designed to compensate for pupil centroid shift and cycloration, both of Which may occur because of patient characteristics and the different environments at the time of measurement and at the time of treatment.
FDA Recall
Terminated
·AMO Manufacturing USA, LLC·Product code LZS·July 18, 2011
STAR S4 IR Excimer Laser System; Software Version 5.02 Mfg by : AMO Manufacturing USA, LLC 510 Cottonwood Drive Milpitas, CA 95035 Iris registration is designed to compensate for pupil centroid shift and cycloration, both of Which may occur because of patient characteristics and the different environments at the time of measurement and at the time of treatment.
FDA Recall
Terminated
·AMO Manufacturing USA, LLC·Product code LZS·July 18, 2011
Nidek Excimer Laser Corneal Surgery System, model EC-5000 CXIII. Opthalmic Device. The system is composed as a laser generator which produces an excimer laser radiation of wavelength 193nm, a beam delivery unit, an optical system for observation, a gas system and a computer for system control.
FDA Recall
Terminated
·Nidek Inc·Product code LZS·August 6, 2012
EC-5000 Excimer Laser Corneal Surgery System (EC-5000, EC 5000 CXIII, EC-5000 Quest. Opthalmic: NIDEK EXCIMER LASER CORNEAL SURGERY SYSTEM, model EC-5000, is an ophthalmic laser system used for correction of corneal refraction and ablation of the corneal surface.
FDA Recall
Terminated
·Nidek Inc·Product code LZS·March 24, 2015