Model note · Retinal Laser

Ellex Integre Pro Scan pattern scanning photocoagulator

Name: Ellex Integre Pro Scan pattern scanning photocoagulator
Brand: Integre Pro Scan

The Integre Pro Scan is an all in one slit lamp and laser photocoagulator, with the laser cavity built into the slit lamp table rather than a separate console. It offers single spot treatment and pattern scanning for panretinal photocoagulation, controlled from a tablet style interface. It comes in green 532 nm, yellow 561 nm or yellow and red configurations; this note focuses on the green version.

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The model

Maker, model and type.

Maker: Ellex Medical Pty Ltd, now Lumibird Medical
Model: Integre Pro Scan pattern scanning photocoagulator (green 532 nm configuration, LP6G)
Device type: Retinal Laser
Main document: Open the public document

Key specifications

What the public record says.

Item	Value	Source
Wavelength options	Green 532 nm; yellow 561 nm; yellow and red 561 and 670 nm	Source
Power at fibre port	Green 1.5 W (yellow 1.5 W, red 1 W)	Source
Power at cornea	Green 50 to 1500 mW	Source
Exposure time	Pattern scanning 10 to 30 ms; single spot 10 ms to 8.0 s	Source
Spot size	Pattern scanning 100 to 500 micrometres; single spot 50 to 1000, continuously variable	Source
Aiming beam	Red 635 nm, adjustable intensity, Class 2 below 1 mW	Source
Laser class	Class 4; Nd:DPSS 532 nm, 2 W maximum	Source
Electrical and cooling	100 to 240 VAC, 50/60 Hz, 800 VA; air cooled	Source
Slit lamp magnification	6x, 10x, 16x, 25x, 40x	Source
Weight and size	35 kg (laser only); 62 x 76 x 47 cm	Source

Recalls

Known FDA recalls.

Z-1971-20232023-03-16
Integre Pro and Pro Scan models including Pro Scan Green LP6G: with an LIO fitted, scattered beam could exit through the slit lamp port.
FDA record

Safety

Safety warnings from the record.

With an LIO connected, scattered laser light could leave through the slit lamp objective lens when firing, exposing people near the slit lamp. Source
This is a Class 4 laser product; avoid exposure to direct or scattered radiation. Source

Sources

Where this note comes from.

Not covered: The FDA file for K142398 holds only the decision letter, not a technical summary. No operator or service manual was found, so error codes, calibration and maintenance intervals are missing. Brochure specifications vary slightly between Lumibird documents (for example green power at the fibre port), and the 2026 brochure was used.

BMEssentia knowledge drafted from public information, reviewed by Hasan Khaled Ismail on 2026-10-24. Always follow the manufacturer's instructions for use and service manual.

Retinal Laser