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i-Lumen Scientific

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uuid0002sti

Namestring
i-Lumen Scientific
Legal namestring
i-Lumen Scientific, Inc.
Websiteurl
i-lumen.com
Company typeenum
Private
Founded yearint
2015
Descriptiontext

i-Lumen Scientific, Inc. is a Bloomington, Minnesota-based clinical-stage medical device company developing the i-LUMEN AMD System, a non-invasive bioelectric therapy intended to restore retinal electrophysiology in patients with intermediate to advanced dry age-related macular degeneration (AMD). The device delivers a proprietary dual waveform (monophasic and biphasic) microcurrent through the closed eyelid during an in-office treatment, with the stated mechanism of restoring the retinal pigment epithelium's transepithelial potential (TEP) and increasing production of pigment epithelium-derived factor (PEDF), a signaling protein associated with photoreceptor survival. The therapy does not require anesthesia or incisions and is administered in 7 treatments over approximately 2 months, with pilot data showing a 9.6-letter mean improvement in best-corrected visual acuity versus 6.3 letters reported for a competing energy-based dry AMD device.

The company is currently conducting the i-SIGHT2 pivotal trial across the United States, United Kingdom, Australia, and New Zealand, targeting 120 participants with primary endpoint data expected in early 2028. The U.S. arm was enabled by an FDA Investigational Device Exemption (IDE) approval received in March 2026, with the first U.S. patient randomized at Texas Retina Associates in July 2026. Earlier clinical work includes the multicenter i-SIGHT pilot, a decade-long open-label evaluation (2014–2024), preclinical studies at Schepens Eye Institute, and computational modeling of current distribution across ocular tissues. The scientific foundation spans more than 30 years of bioelectric-stimulation research, led by CEO John Velure (prior neurostimulation exits including Neurotech and Compex Technologies) and supported by an advisory board that includes senior ophthalmology and electrophysiology researchers from Mayo Clinic, Harvard/Mass Eye and Ear, and Kings College.

i-Lumen Scientific is pre-commercial: the device is investigational only, no pricing exists, and revenue is not yet generated. The go-to-market model, once approved, is enterprise/field sales targeting ophthalmologists and retina specialists who treat dry AMD patients across in-office clinical settings in the U.S. and international markets. To date the company has raised approximately $18.8 million in disclosed funding (a $750,000 round in 2020 and approximately $18.0 million in 2022), with a Series B referenced on the investor site but not yet disclosed. Board composition includes Robert Warner (former Alcon Laboratories President) and Stella Robertson of Bios Partners, providing sector-experienced governance. The strategic backdrop is reinforced by Alcon's $850 million acquisition of a competing bioelectric dry AMD device (Valeda) in late 2025, establishing a comparable exit valuation benchmark.

Short descriptiontext

i-Lumen Scientific is a clinical-stage medical device company developing the i-LUMEN AMD System, a non-invasive bioelectric stimulation therapy for intermediate to advanced dry age-related macular degeneration, currently in a multinational pivotal trial targeting ophthalmologists and retina specialists.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
1–10
akta.pro rankint
HeadquartersBloomington, United States
HQ citystring
Bloomington
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices1 record

Each record includes

City, Country, Type, Description, Source

Keyword5 values
bioelectric stimulation therapy, dry AMD treatment, retinal electrophysiology therapy, non-invasive medical devices, ophthalmic microcurrent therapy
Industry2 codes
1Cataract Surgery Systems & IOLs (Phaco Systems, IOLs, Intraoperative Aberrometry, Viscoelastics)
CodeHLAHAJAHPrimaryYes
2Vitreoretinal Surgical Devices (Vitrectomy Systems, Endolaser, Illumination, Tamponades)
CodeHLAHAJAJPrimaryNo
NAICS code2 codes
  • Electromedical and Electrotherapeutic Apparatus Manufacturing334510
  • Surgical and Medical Instrument Manufacturing339112
SIC code2 codes
  • Electromedical & Electrotherapeutic Apparatus3845
  • Surgical & Medical Instruments & Apparatus3841
Product category
Ophthalmic Medical Devices
No data
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model1 record
1Pre-commercial (Clinical Stage)
TypeHardware Sales
Description

i-Lumen Scientific is a clinical-stage company. The i-LUMEN AMD System is an investigational device limited by Federal (or United States) law for investigational use only. The company is currently conducting the i-SIGHT2 pivotal clinical trial and has not yet commercialized its product. Revenue will be generated following successful regulatory approvals.

i-lumen.com
Marketing channels5 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels1 record

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components5 values
Technology or R&D, Personnel, Operations, Marketing or Sales, Others
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Brand1 record
1i-LUMEN AMD System
Description

Non-invasive bioelectric therapy system delivering microcurrent stimulation through the eyelid to restore retinal electrophysiology in patients with intermediate to advanced dry AMD.

i-lumen.com
Core offering1 text field

i-Lumen Scientific develops the i-LUMEN AMD System, a non-invasive bioelectric stimulation medical device that delivers proprietary dual waveform microcurrent through the closed eyelid to restore transepithelial potential across the retinal pigment epithelium. The investigational device targets intermediate to advanced dry age-related macular degeneration and is administered in-office by ophthalmologists and retina specialists without anesthesia or incisions.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 5 values shown
  • 61.5% of patients achieved ≥10 letter improvement in BCVA by month 2
+4 more records
Product overview1 text field

i-Lumen Scientific offers a single core product: the i-LUMEN AMD System®, a non-invasive bioelectric therapy medical device. The system uses a proprietary dual waveform algorithm delivering microcurrent stimulation through the eyelid to restore retinal electrophysiology in patients with intermediate to advanced dry AMD. The company is supported by its clinical research program, including the completed i-SIGHT study and the ongoing i-SIGHT2 pivotal study (ClinicalTrials.gov: NCT05447650, NCT06662162).

Product and service1 record
1i-LUMEN AMD System®
CategoryInvestigational Ophthalmic Medical Device
Description

A non-invasive bioelectric therapy medical device that delivers proprietary dual waveform microcurrent stimulation through the closed eyelid to restore transepithelial potential (TEP) across the retinal pigment epithelium, improve photoreceptor function, and support visual acuity in patients with intermediate to advanced dry age-related macular degeneration. It is administered in-office by ophthalmologists and retina specialists without anesthesia or incisions.

Scale indicator8 records

Each record includes

Type, Value, Description, Source

Partnership2 partners
Strategic tierCoreTypeStrategic or Co-development Partner
Description

i-SIGHT2 pivotal clinical study is being conducted at clinical trial sites across four countries including Texas Retina Associates in the US and London North West University Healthcare NHS Trust in the UK. These clinical partnerships are essential for regulatory approval pathway.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

Preclinical research studies were conducted at Schepens Eye Institute evaluating neuroprotective signaling, photoreceptor survival, and inflammatory pathway modulation as part of the scientific foundation for the bioelectric therapy.

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
TypeBroad incumbent
Description

Global ophthalmology leader that acquired LumiThera's Valeda system for $850M in late 2025, establishing the strategic acquisition benchmark for non-invasive dry AMD devices and representing both a competitor and potential acquirer of i-Lumen.

TypeDirect peer
Description

Developer of the Valeda Light Delivery System, a non-invasive photobiomodulation device for dry AMD and the closest direct competitor to i-Lumen's i-LUMEN AMD System in the energy-based dry AMD device category.

TypeBroad incumbent
Description

Acquired Iveric Bio and now markets Izervay (avacincaptad pegol), the second approved complement inhibitor for geographic atrophy, directly competing for the same advanced dry AMD patient population.

TypeEmerging player
Description

Clinical-stage gene therapy company developing ADVM-022 (ixoberogene soroparvovec) for wet AMD, representing a potential future paradigm shift that could compete with or complement device-based dry AMD therapies.

TypeBroad incumbent
Description

Developer of Eylea (aflibercept), the standard-of-care anti-VEGF therapy for wet AMD and a major player in retinal disease whose physician relationships and commercial reach shape the dry AMD treatment landscape.

TypeBroad incumbent
Description

Global pharmaceutical company with a major ophthalmology franchise including Lucentis and Beovu, and the resources to acquire or compete with emerging dry AMD device and therapy developers.

TypeBroad incumbent
Description

Developer of Lucentis (ranibizumab) and a long-standing leader in retinal therapeutics, with extensive retina specialist relationships and ongoing pipeline programs in AMD.

TypeBroad incumbent
Description

Developer of Syfovre (pegcetacoplan), the first FDA-approved complement inhibitor for geographic atrophy (advanced dry AMD) — a drug competitor that defines the standard of care i-Lumen's device must outperform or complement.

TypeEmerging player
Description

Clinical-stage ophthalmology company developing sustained-release therapies for retinal diseases including wet AMD, with overlapping customer base of retina specialists who would also prescribe i-LUMEN.

TypeBroad incumbent
Description

Diversified ophthalmology company with retinal surgery and pharmaceutical offerings, and a potential strategic acquirer or distribution partner for novel dry AMD devices.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat4 records

Each record includes

Type, Details

Key risks6 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers2 records

Each record includes

Name, Industry, Type, Use case, Source, UUID

Segment3 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile2 records

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
Yes
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature3 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles13 records

Each record includes

Name, Designation, Designation category, Overview, Profile commentary, Source

No data
No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds2 records

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

i-Lumen Scientific

Ophthalmic Medical Devicesi-lumen.com

i-Lumen Scientific is a clinical-stage medical device company developing the i-LUMEN AMD System, a non-invasive bioelectric stimulation therapy for intermediate to advanced dry age-related macular degeneration, currently in a multinational pivotal trial targeting ophthalmologists and retina specialists.

What i-Lumen Scientific does

i-Lumen Scientific, Inc. is a Bloomington, Minnesota-based clinical-stage medical device company developing the i-LUMEN AMD System, a non-invasive bioelectric therapy intended to restore retinal electrophysiology in patients with intermediate to advanced dry age-related macular degeneration (AMD). The device delivers a proprietary dual waveform (monophasic and biphasic) microcurrent through the closed eyelid during an in-office treatment, with the stated mechanism of restoring the retinal pigment epithelium's transepithelial potential (TEP) and increasing production of pigment epithelium-derived factor (PEDF), a signaling protein associated with photoreceptor survival. The therapy does not require anesthesia or incisions and is administered in 7 treatments over approximately 2 months, with pilot data showing a 9.6-letter mean improvement in best-corrected visual acuity versus 6.3 letters reported for a competing energy-based dry AMD device.

The company is currently conducting the i-SIGHT2 pivotal trial across the United States, United Kingdom, Australia, and New Zealand, targeting 120 participants with primary endpoint data expected in early 2028. The U.S. arm was enabled by an FDA Investigational Device Exemption (IDE) approval received in March 2026, with the first U.S. patient randomized at Texas Retina Associates in July 2026. Earlier clinical work includes the multicenter i-SIGHT pilot, a decade-long open-label evaluation (2014–2024), preclinical studies at Schepens Eye Institute, and computational modeling of current distribution across ocular tissues. The scientific foundation spans more than 30 years of bioelectric-stimulation research, led by CEO John Velure (prior neurostimulation exits including Neurotech and Compex Technologies) and supported by an advisory board that includes senior ophthalmology and electrophysiology researchers from Mayo Clinic, Harvard/Mass Eye and Ear, and Kings College.

i-Lumen Scientific is pre-commercial: the device is investigational only, no pricing exists, and revenue is not yet generated. The go-to-market model, once approved, is enterprise/field sales targeting ophthalmologists and retina specialists who treat dry AMD patients across in-office clinical settings in the U.S. and international markets. To date the company has raised approximately $18.8 million in disclosed funding (a $750,000 round in 2020 and approximately $18.0 million in 2022), with a Series B referenced on the investor site but not yet disclosed. Board composition includes Robert Warner (former Alcon Laboratories President) and Stella Robertson of Bios Partners, providing sector-experienced governance. The strategic backdrop is reinforced by Alcon's $850 million acquisition of a competing bioelectric dry AMD device (Valeda) in late 2025, establishing a comparable exit valuation benchmark.

i-Lumen Scientific firmographics

Firmographics
Name
i-Lumen Scientific
Legal name
i-Lumen Scientific, Inc.
Website
https://i-lumen.com
Company type
Private
Founded year
2015
Operating status
Operating
Headcount range
1–10 employees
Short description
i-Lumen Scientific is a clinical-stage medical device company developing the i-LUMEN AMD System, a non-invasive bioelectric stimulation therapy for intermediate to advanced dry age-related macular degeneration, currently in a multinational pivotal trial targeting ophthalmologists and retina specialists.
Ownership category
akta.pro rank

i-Lumen Scientific industry classification

Industry
Product category
Ophthalmic Medical Devices
NAICS
Electromedical and Electrotherapeutic Apparatus Manufacturing (334510), Surgical and Medical Instrument Manufacturing (339112)
SIC
Electromedical & Electrotherapeutic Apparatus (3845), Surgical & Medical Instruments & Apparatus (3841)
akta.pro primary industry
Cataract Surgery Systems & IOLs (Phaco Systems, IOLs, Intraoperative Aberrometry, Viscoelastics) (HLAHAJAH)
akta.pro secondary industry
Vitreoretinal Surgical Devices (Vitrectomy Systems, Endolaser, Illumination, Tamponades) (HLAHAJAJ)

Keywords

  • Bioelectric stimulation therapy
  • Dry AMD treatment
  • Retinal electrophysiology therapy
  • Non-invasive medical devices
  • Ophthalmic microcurrent therapy

Where i-Lumen Scientific is headquartered

Location

Headquarters

HQ city
Bloomington
HQ country
United States
HQ region
North America

Offices1 record

Markets served

i-Lumen Scientific business model

Business model
GTM type
B2B
Offering type
Hardware or Manufacturing
Cost components
Technology or R&D, Personnel, Operations, Marketing or Sales, Others

Revenue model

  1. Pre-commercial (Clinical Stage): i-Lumen Scientific is a clinical-stage company. The i-LUMEN AMD System is an investigational device limited by Federal (or United States) law for investigational use only. The company is currently conducting the i-SIGHT2 pivotal clinical trial and has not yet commercialized its product. Revenue will be generated following successful regulatory approvals.

Go-to-market motion1 record

Distribution channels1 record

Marketing channels5 records

i-Lumen Scientific product offering

Product offering

Core offering

i-Lumen Scientific develops the i-LUMEN AMD System, a non-invasive bioelectric stimulation medical device that delivers proprietary dual waveform microcurrent through the closed eyelid to restore transepithelial potential across the retinal pigment epithelium. The investigational device targets intermediate to advanced dry age-related macular degeneration and is administered in-office by ophthalmologists and retina specialists without anesthesia or incisions.

Product overview

i-Lumen Scientific offers a single core product: the i-LUMEN AMD System®, a non-invasive bioelectric therapy medical device. The system uses a proprietary dual waveform algorithm delivering microcurrent stimulation through the eyelid to restore retinal electrophysiology in patients with intermediate to advanced dry AMD. The company is supported by its clinical research program, including the completed i-SIGHT study and the ongoing i-SIGHT2 pivotal study (ClinicalTrials.gov: NCT05447650, NCT06662162).

Differentiator

Problem solved

Functional benefit

Brands

  • i-LUMEN AMD System: Non-invasive bioelectric therapy system delivering microcurrent stimulation through the eyelid to restore retinal electrophysiology in patients with intermediate to advanced dry AMD.

Products and services

  • i-LUMEN AMD System® A non-invasive bioelectric therapy medical device that delivers proprietary dual waveform microcurrent stimulation through the closed eyelid to restore transepithelial potential (TEP) across the retinal pigment epithelium, improve photoreceptor function, and support visual acuity in patients with intermediate to advanced dry age-related macular degeneration. It is administered in-office by ophthalmologists and retina specialists without anesthesia or incisions.

Quantifiable outcome

  • 61.5% of patients achieved ≥10 letter improvement in BCVA by month 2
  • +4 more outcomes

Companies that use i-Lumen Scientific

Customer profile

Named customers2 records

Segments3 records

Ideal customer profiles2 records

i-Lumen Scientific technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature3 records

i-Lumen Scientific partnerships and signals

Strategic signal

Partnerships

Two partnerships are on record, tiered core.

  • Clinical Trial Sites (US, UK, Australia, New Zealand)coreStrategic or Co-development Partneri-SIGHT2 pivotal clinical study is being conducted at clinical trial sites across four countries including Texas Retina Associates in the US and London North West University Healthcare NHS Trust in the UK. These clinical partnerships are essential for regulatory approval pathway.
  • Schepens Eye InstitutecoreStrategic or Co-development PartnerPreclinical research studies were conducted at Schepens Eye Institute evaluating neuroprotective signaling, photoreceptor survival, and inflammatory pathway modulation as part of the scientific foundation for the bioelectric therapy.

Scale indicators8 records

Recent moves6 records

Expansion highlights6 records

i-Lumen Scientific competitors and assessment

Company assessment

Broad incumbents

  • Alcon: Global ophthalmology leader that acquired LumiThera's Valeda system for $850M in late 2025, establishing the strategic acquisition benchmark for non-invasive dry AMD devices and representing both a competitor and potential acquirer of i-Lumen.
  • Astellas Pharma: Acquired Iveric Bio and now markets Izervay (avacincaptad pegol), the second approved complement inhibitor for geographic atrophy, directly competing for the same advanced dry AMD patient population.
  • Regeneron: Developer of Eylea (aflibercept), the standard-of-care anti-VEGF therapy for wet AMD and a major player in retinal disease whose physician relationships and commercial reach shape the dry AMD treatment landscape.
  • Novartis: Global pharmaceutical company with a major ophthalmology franchise including Lucentis and Beovu, and the resources to acquire or compete with emerging dry AMD device and therapy developers.
  • Genentech (Roche): Developer of Lucentis (ranibizumab) and a long-standing leader in retinal therapeutics, with extensive retina specialist relationships and ongoing pipeline programs in AMD.
  • Apellis Pharmaceuticals: Developer of Syfovre (pegcetacoplan), the first FDA-approved complement inhibitor for geographic atrophy (advanced dry AMD) — a drug competitor that defines the standard of care i-Lumen's device must outperform or complement.
  • Bausch + Lomb: Diversified ophthalmology company with retinal surgery and pharmaceutical offerings, and a potential strategic acquirer or distribution partner for novel dry AMD devices.

Direct peers

  • LumiThera: Developer of the Valeda Light Delivery System, a non-invasive photobiomodulation device for dry AMD and the closest direct competitor to i-Lumen's i-LUMEN AMD System in the energy-based dry AMD device category.

Emerging players

  • Adverum Biotechnologies: Clinical-stage gene therapy company developing ADVM-022 (ixoberogene soroparvovec) for wet AMD, representing a potential future paradigm shift that could compete with or complement device-based dry AMD therapies.
  • Ocular Therapeutix: Clinical-stage ophthalmology company developing sustained-release therapies for retinal diseases including wet AMD, with overlapping customer base of retina specialists who would also prescribe i-LUMEN.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat4 records

Key risks6 records

Key highlights7 records

Customer concentration

i-Lumen Scientific financial estimates

Financial estimate

Revenue estimate

Valuation estimate

i-Lumen Scientific leadership team

Management profile

Number of profiles

Profiles13 records

i-Lumen Scientific funding detail

Funding detail

Funding overview

Funding rounds2 records

Investors

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

i-Lumen Scientific M&A and investment

M&A and investment

M&A

Investments

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Frequently asked questions about i-Lumen Scientific

What does i-Lumen Scientific do?

i-Lumen Scientific develops the i-LUMEN AMD System, a non-invasive bioelectric stimulation medical device that delivers proprietary dual waveform microcurrent through the closed eyelid to restore transepithelial potential across the retinal pigment epithelium. The investigational device targets intermediate to advanced dry age-related macular degeneration and is administered in-office by ophthalmologists and retina specialists without anesthesia or incisions.

Is i-Lumen Scientific a public or private company?

i-Lumen Scientific is a private company. It is classified as venture growth investor backed and is currently operating.

When was i-Lumen Scientific founded?

i-Lumen Scientific was founded in 2015. It employs 1 to 10 people.

Where is i-Lumen Scientific based?

i-Lumen Scientific is headquartered in Bloomington, United States, in the North America region.

How does i-Lumen Scientific make money?

One revenue line is on record: pre-commercial (Clinical Stage).

Who are i-Lumen Scientific's main competitors?

Broad incumbents on record are Alcon, Astellas Pharma, Regeneron, Novartis, Genentech (Roche), Apellis Pharmaceuticals and Bausch + Lomb. LumiThera is listed as a direct peer. Emerging players are Adverum Biotechnologies and Ocular Therapeutix.

Does i-Lumen Scientific have an API?

No public API is recorded for i-Lumen Scientific.

What industry is i-Lumen Scientific in?

i-Lumen Scientific's product category is Ophthalmic Medical Devices. Its primary akta.pro industry code is HLAHAJAH, Cataract Surgery Systems & IOLs (Phaco Systems, IOLs, Intraoperative Aberrometry, Viscoelastics), with a secondary code of HLAHAJAJ, Vitreoretinal Surgical Devices (Vitrectomy Systems, Endolaser, Illumination, Tamponades). Its NAICS code is 334510 and its SIC code is 3845.

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Live signals
Longevity.TechnologyFirst U.S. patient enrolled in clinical trial for new dry AMD vision treatmenti-Lumen Scientific announced that the first U.S. patient was randomized in the i-SIGHT2 pivotal study evaluating the i-Lumen AMD System for intermediate to advanced dry age-related macular degeneration, with the procedure performed at Texas Retina Associates in Fort Worth, Texas. The study, which had already begun in the United Kingdom, represents the start of U.S. participation in this global clinical program for the investigational bioelectric therapy that delivers low-level microcurrent stimulation through the eyelid to improve photoreceptor function.PR Newswirei-Lumen Scientific Announces First U.S. Patient Randomized in i-SIGHT2 Pivotal Study Evaluating Noninvasive Bioelectric Therapy for Intermediate to Advanced Dry AMDi-Lumen Scientific announced the first U.S. patient randomized in the i-SIGHT2 pivotal study for intermediate to advanced dry AMD, at Texas Retina Associates in Fort Worth. The randomized, sham-controlled trial evaluates the i-Lumen AMD System's noninvasive bioelectric therapy. The device is investigational and not FDA-approved.EIN Presswirei-Lumen Scientific Announces 1st U.S. Patient Randomized in i-SIGHT2 Pivotal Study for Intermediate to Advanced Dry AMDi-Lumen Scientific announced the first U.S. patient randomized in the i-SIGHT2 pivotal study for intermediate to advanced dry AMD, at Texas Retina Associates in Fort Worth, TX. The randomized, sham-controlled trial evaluates the i-Lumen AMD System's bioelectric therapy to improve retinal electrophysiology and visual function. The device is investigational and not FDA-approved.Longevity.TechnologyI-Lumen receives FDA IDE to start US i-SIGHT2 enrollmentI-Lumen Scientific received FDA IDE approval to initiate U.S. enrollment in the i-SIGHT2 pivotal clinical trial for its non-invasive bioelectric stimulation therapy treating intermediate to advanced dry age-related macular degeneration. The multinational study, already enrolling participants in the United Kingdom, Australia, and New Zealand, will include 120 patients total with U.S. enrollment anticipated to begin in late April 2026. Positive efficacy and safety results from the trial could support regulatory submissions for U.S. and international commercialization.PR Newswirei-Lumen Scientific Receives FDA Approval of IDE to Initiate U.S. Enrollment in i-SIGHT2 Clinical Study for dry AMDi-Lumen Scientific has received Investigational Device Exemption (IDE) approval from the FDA to expand its i-SIGHT2 Pivotal Study for a non-invasive bioelectric stimulation therapy treating intermediate to advanced dry age-related macular degeneration (AMD) to the United States. The global clinical trial, already enrolling participants in the United Kingdom, Australia, and New Zealand, plans to enroll 120 participants total, with U.S. enrollment anticipated to begin in late April 2026. The first participant has been treated in the UK, and if successful, the therapy could support regulatory submission for commercialization in the U.S. and international markets.PR Newswirei-Lumen Scientific Receives FDA Approval of IDE to Initiate U.S. Enrollment in i-SIGHT2 Clinical Study for dry AMDi-Lumen Scientific has received FDA Investigational Device Exemption approval to expand its i-SIGHT2 pivotal clinical study for a non-invasive bioelectric stimulation therapy targeting intermediate to advanced dry age-related macular degeneration to the United States. The first study participant has already been treated in the United Kingdom at London North West University Healthcare NHS Trust, with the global trial also actively enrolling in Australia and New Zealand. The study plans to enroll 120 participants total, with U.S. enrollment anticipated to begin in late April 2026, and if successful, could support regulatory submission for commercialization in the U.S. and international markets.SecSEC FORM Di-Lumen Scientific, Inc. filed a Form D with the SEC on April 26, 2022, announcing an exempt securities offering under Rule 506(b). The company reported total offering and sales amounts of approximately $18 million, with $500,000 remaining to be sold.