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Omni Cross Linking Device

Omni Cross Linking Device

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Corneal collagen cross-linking is a
technique which uses UV light and a
photosensitizer to strengthen chemical
bonds in the cornea. The goal of the
treatment is to halt progressive and
irregular changes in corneal shape known
as ectasia. These ectatic changes are
typically marked by corneal thinning and
an increase in the anterior and/or posterior
curvatures of the cornea, and often lead
to high levels of myopia and astigmatism.
The most common form of ectasia is
keratoconus and less often ectasia is seen
after laser vision correction such as LASIK.
Corneal Cross Linking is a process of
photopolymerization. During this process
of photopolymerization, singlet oxygen is
being created with the use of riboflavin
as a photomediator activated by UV-light.
Free radicals lead to physical intra- and
interhelical cross links of stromal collagen
fibers. This process takes place mainly in
the anterior 200μ to 250μ of the stroma.
This is important to remember in cases
where a refractive procedure is planned
post-XL.

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Technical Specifications

UV Wavelength

365 nm

Intensity Range

3 mW/cm² to 45 mW/cm² continuously adjustable

Working Distance

Approximately 50 mm ± 5 mm

Fixation Light

Adjustable brightness to maintain stability

Tracking Area

Customizable threshold zone; system auto‑pauses if exceeded

Delivery Modes

Continuous, pulsed (to reduce heating risk), and LASIK-specific radiation delivery

Special Features & Treatment Options

Fully Customizable UV Settings

Energy range spans 3 mW/cm² to 45 mW/cm², adjustable in 1 mW steps. Supports continuous, pulsed, or LASIK CXL modes tailored to clinical needs, including infectious keratitis.

Built‑in Eye Tracking & Calibration

Infrared eye tracking ensures correct treatment distance and patient fixation. The system automatically halts if the eye moves outside the set threshold. Continuous light intensity monitoring ensures dosing accuracy throughout procedures.

Optional Integrated Pachymeter

Corneal pachymetry can be built in, allowing the system to recommend riboflavin application parameters based on thickness and anatomical data.

Intuitive Touchscreen Interface

7‑inch color touch display shows treatment settings, eye monitoring, and remaining time. Real‑time data and patient info can be exported via Wi‑Fi or Bluetooth as PDF or printed externally.