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. 2023 Nov 23;9:73. doi: 10.1186/s40942-023-00498-1

Table 2.

Epiretinal device characteristics

Device Electrode specifications Implant Size Benefits Reported SAE/AE’s Clinical Status
NR600 600 3D microelectrodes (typical length of 150 ± 30 µm, and a maximum exposed tip height of 50 µm) Three different lengths available varying between 20 and 26 mm in axial lengths

- Porous and chemically stable electrode material

- Passivation layer to minimize shunting currents

and limit electrode active area stimulation

- Configurable settings

- Lower peak intensity

- No need for surplus wiring outside the eye

- Relatively low risk procedure

- Fast healing and recovery time

- Mild corneal edema along with slightly elevated intra-ocular pressure

- Intra ocular lens luxation with subsequent elevated IOP

In clinical trials available in Italy, Israel, and Belgium
IMIE 256 256 electrodes: two sizes of disc-shaped electrode diameters including 248 large electrodes (210 µm in diameter) and 8 smaller electrodes (160 µm in diameter) 2 sizes: Area covers 4.75 mm × 6.50 mm center-to-center pitch is 350 µm for the large electrodes and 300 µm for the small electrodes

- Reduced risk of episcleral electronics capsule

exposure

- Greater density of functioning electrodes

- 100% of subjects implanted performed better on

visual tests with the system on versus off.

- Compact size matching retinal curvature

- Low power consumption

- Reduced dissipated heat to surrounding tissue

- Multiple layers of biocompatible and durable

barrier material to withstand bodily fluid corrosion

- Improved manufacturability for mass production

allowing for future reduced costs [1

- Device displaced slightly toward the upper

temporal position in the macula

- low intraocular pressure in the implanted eye 6 weeks after repositioning

Future clinical trials for testing in more patients over a longer follow-up period
POLYRETINA 2215 stimulating pixels (80 and 130 µm diameter) 24 mm axially × 24 mm laterally × 14 mm wide

- Extra layer of PDMS substrate material to reduce

strain

- Foldable for implantation ease

- Hemisphere shape matching retinal curvature

- Reduced retinal tissue heating

- Homogeneous temperature distribution during

deposition

- Large diameter of photovoltaic electrodes

- Preserved high deformability

- low level of acute immune response activation

Information not available In vivo study showed that it restores light-evoked cortical responses at safe irradiance levels and is tolerable after two weeks if implantation
EPI-RET3

25 electrodes

(100 µm diameter)

40 mm length × 3 mm width

- Wireless implant

- Short surgical time

- Direct electrode to retinal stimulation

- Four cases (three mild and one moderate) of non-progressive epiretinal gliosis at the tack fixation site

- Inflammatory reaction in the implanted eye due to corneal sutures

- Slight decline in residual visual perception in two patients post implant removal of the implanted eye

- Minor choroidal atrophy within the area where the retinal tacks had been placed

- removal of the implant had caused a retinal break (treated with laser coagulation and silicone oil tamponade)

- acute sterile hypopyon after implantation

- a thick epiretinal membrane in the tack area at the retinal center

Six patients were implanted for 28 days.

No active clinical trials at this time