QMAX · Glaucoma

QMAX: the two-pressure glaucoma implant.

Equalizing pressure across the optic nerve head.

Glaucoma damages the optic nerve through a pressure gradient between the inside of the eye and the fluid around the nerve. QMAX is a first-in-class implant designed to neutralize that gradient.

Illustration of QMAX routing fluid to equalize pressure across the optic nerve.

The translaminar pressure gradientTranslaminar pressure gradientThe pressure difference across the optic nerve head between IOP and CSF pressure. A sustained gradient strains nerve fibers.

The optic nerve headOptic nerve headWhere retinal nerve fibers exit the eye. QMAX is designed to relieve strain at this point. sits at the lamina cribrosa, a thin sheet of nerve fibers under load from two sides: intraocular pressure (IOPIntraocular pressureFluid pressure inside the eye. Most glaucoma therapies aim to lower IOP.) in front and the cerebrospinal fluid pressure in the space behind the nerve. What strains and damages the nerve is the difference between them, the translaminar pressure gradientTranslaminar pressure gradientThe pressure difference across the optic nerve head between IOP and CSF pressure. A sustained gradient strains nerve fibers.. Lowering IOPIntraocular pressureFluid pressure inside the eye. Most glaucoma therapies aim to lower IOP. alone narrows that gap from one side only. If the gradient remains, nerve fibers keep dying.

What QMAX does

  • Connects the aqueous humor to the fluid space around the optic nerve

  • Equalizes pressure across the optic nerve headOptic nerve headWhere retinal nerve fibers exit the eye. QMAX is designed to relieve strain at this point., not only inside the eye

  • Removes the gradient that strains and kills retinal ganglion cell axons

  • Operates without a filtering bleb and without anti-fibrotic agents

  • Targets both high-IOPIntraocular pressureFluid pressure inside the eye. Most glaucoma therapies aim to lower IOP. and normal-tension glaucoma populations (investigator context; not labeling)

Illustration of intraocular and cerebrospinal fluid pressure opposing at the optic nerve head.

What QMAX is not

Not a trabecular shunt.

It does not depend on Schlemm's canal.

Not a bleb-based filter.

No subconjunctival blister, no bleb revision.

Not an IOPIntraocular pressureFluid pressure inside the eye. Most glaucoma therapies aim to lower IOP.-only device.

It is built around the gradient, not the symptom.

The result is a device that addresses what other surgeries leave on the table, including the patients whose vision keeps dropping at "normal" pressures.

Clinical illustration of a filtering bleb after conventional glaucoma surgery.
QSCOPE single-use endoscopic delivery system.

Built for the surgical workflow you already run

QMAX is delivered with QSCOPE, a single-use endoscopic system that gently tents the nerve sheath into a protected space and places the implant. It is designed as a simple, repeatable endoscopic procedure that integrates with existing cataract capital equipment, rather than a delicate open dissection.

Designed to be

  • Simple and repeatable

  • Endoscopic

  • High-turnover workflow compatible

  • Free of post-op bleb management

Route to market

QMAX is on a defined regulatory and clinical pathway toward US market access. The milestones below are forward-looking and subject to change; they are presented for investor and partner context, not as guarantees.

  1. 2026

    FDA Breakthrough Device application (targeted)

  2. 2026

    Gen 3 clinical study

  3. 2027

    Endoscopic delivery feasibility study

  4. 2028

    GLP preclinical · FDA IDE

  5. 2028–2030

    Pivotal trial

  6. 2030

    FDA approval (De Novo) (targeted)

What leaders in glaucoma are saying

Named advisors have reviewed QMAX. Their endorsing statements will be published following clearance.

John Berdahl, MD

Endorsement pending final approval.

Richard Beckman, MD

Endorsement pending final approval.

Reay Brown, MD

Endorsement pending final approval.

The science behind the device

  • 10 global patent families covering the ONSAS mechanism, the device and delivery system, and the surgical method

  • First-in-human experience across three device generations, engineering out failure modes generation by generation

  • Clinical pathway routed through US sites