15 results
·
41ms
·
Sources: EU EUDAMED, US FDA
RAINDROP NEAR VISION INLAY
FDA Adverse Event
Injury
·Product code LQE·June 2, 2022
RAINDROP CORNEAL INLAY
FDA Adverse Event
Injury
·RVO 2.0, INC.·Product code LQE·May 23, 2024
RAINDROP INLAY
FDA Adverse Event
Injury
·RVO 2.0, INC.·Product code LQE·March 29, 2019
RAIN DROP NEAR VISION INLAY
FDA Adverse Event
Malfunction
·RVO 2.0, INC·Product code LQE·December 19, 2019
RAINDROP IMPLANT
FDA Adverse Event
Injury
·REVISION / RVO 2.0, INC.·Product code LQE·October 13, 2020
RAINDROP UNDERLAY LENS
FDA Adverse Event
Injury
·REVISION / RVO 2.0, INC.·Product code LQE·October 21, 2019
RAIN DROP CORNEAL INLAY
FDA Adverse Event
Injury
·REVISION OPTICS/ RVO 2.0, INC·Product code LQE·April 3, 2019
RAINDROP CORNEAL INLAY
FDA Adverse Event
Injury
·REVISION OPTICS / RVO 2.0, INC.·Product code LQE·April 4, 2019
RAINDROP INLAY
FDA Adverse Event
Injury
·REVISION OPTICS/RVO 2.0 INC.·Product code LQE·January 22, 2020
RAINDROP INLAY
FDA Adverse Event
Malfunction
·OPTICS MEDICAL / RVO 2.0, INC·Product code LQE·March 16, 2021
RAINDROP INLAY
FDA Adverse Event
Injury
·REVISION OPTICS / RVO 2.0, INC.·Product code LQE·February 8, 2022
RAINDROP INLAY
FDA Adverse Event
Injury
·REVISION OPTICS / RVO 2.0 INC.·Product code LQE·August 13, 2019
RAINDROP NEAR VISION INLAY
FDA Adverse Event
Injury
·REVISION OPTICS, INC. /RVO 2.0, INC.·Product code LQE·September 4, 2019
Raindrop Near Vision Inlay, REF: RD1-1, Sterile, Rx Only, Manufacturer ReVision Optics, Inc.
FDA Recall
Terminated
·RVO 2.0, INC·Product code LQE·November 13, 2018
Raindrop Near Vision Inlay, REF: RD1-1, Sterile, Rx Only, Manufacturer ReVision Optics, Inc.
FDA Enforcement
Class I
·Terminated·RVO 2.0, INC·March 13, 2019