Products information

eyePlate / eyePlate-S

eyePlate

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For IFU in other languages, contact Rheon Medical.

The eyePlate is intended to manage intraocular pressure in glaucoma patients where medically controlled glaucoma or filtering surgery have failed or are likely to fail, such as, but not limited to, neovascular glaucoma, aphakic/pseudophakic glaucoma, uveitic glaucoma, congenital glaucoma, etc.

Conjunctivitis, corneal ulcers, endophthalmitis, orbital cellulitis, bacteremia or septicemia, active scleritis, active uveitis, scleral buckle, rectus muscle surgery.

   The eyePlate is MR safe

eyeWatch implant

eyeWatch

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For IFU in other languages, contact Rheon Medical.

The eyeWatch system is indicated for patients suffering from glaucoma where medical and/or conventional surgical treatments have failed. The eyeWatch system is intended to drain aqueous humor from the anterior chamber to the subconjunctival space and to regulate non-surgically the intraocular pressure during the early post-operative period.

The implantation of the eyeWatch implant is contraindicated if one or more of the following conditions exist:

  • Diagnosis of angle-closure glaucoma, neovascular glaucoma.
  • Patient with ocular malformations such as microphthalmia.
  • Patient with corneal opacifications or irregularities that may interfere with IOP measurements.
  • History of previous corneal transplant surgery.
  • Patient with concurrent inflammatory/infective eye disorder.

The eyewatch is MR Conditional

MR Conditions:

  • Horizontal bore MR system with a static magnetic field of 1.5 Tesla or 3 Tesla.
  •  Gradient magnetic fields lower or equal to 19 T/m.
  • Whole body averaged SAR (Specific Absorption Rate) limited to Normal Operating Mode (WB-SAR ≤2W/kg).
  • The association eyeWatch + eyePlate is expected to produce a maximum temperature rise of 2°C at both 1.5T and 3T for a WB-SAR of 2W/kg after 1h of continuous scanning

Video library

Catagories

Publications

A. Swampillai et al., Int. Ophthalmol., 2025

Short term clinical outcomes of the combined eyeWatch™ implant and eyePlate in refractory glaucoma—a United Kingdom dual centre study

One year clinical outcomes of a dual center study on the eyeWatch system in the United Kingdom.

Singh et al., Journal of Clinical Medicine, 2024

Minimally Invasive Tube Surgery (MITS) – A Novel Method in Glaucoma Drainage Device Implantation

Publication of a new surgical technique for inserting the eyePlate-300 by Dr Faisal Ahmed and his team.

F. Ahmed et al., Journal of Clinical Medecine, 2024

Evaluating the Safety and Efficacy of a Novel Glaucoma Drainage Device in High-Risk Adult Glaucoma Patients: A One-Year Pilot Study

First publication presenting results on the eyePlate-300 used in a standalone fashion (1-year results, 15 patients).

Roy S. and Mermoud A., Journal of Glaucoma, 2023

Efficacy and Safety of an Adjustable Glaucoma Drainage Device (eyewatch System) for Refractory Glaucoma: A 2-Year Prospective Study

Two-year results of the eyeWatch implant combined with an eyePlate implant in refractory glaucoma patients in Lausanne, Switzerland (42 patients).

Elahi et al., Journal of Glaucoma, 2020

EyeWatch Rescue of Refractory Hypotony After Baerveldt Drainage Device Implantation: Description of a new Technique

Case study on the recovery of a failed Baerveldt tube due to hypotony, by implantation of an eyeWatch

Roy et al., European Journal of Ophthalomology, 2020

MRI after successful eyeWatch implantation

Case report of a patient which underwent cerebral MRI after implantation of an eyeWatch device.