Moor Instruments and our sister company in the USA Moor Instruments Inc, are delighted to announce that our newest edition to the Burn Imager family, the moorLDLS-BI rapid line scanner, has successfully gained FDA 510(k) clearance, allowing clinical diagnostic use in the USA. The system already has CE marking, clearing it for clinical diagnosis in Europe too. As with the moorLDI2-BI large area scanner, it has been uniquely recognised by the FDA as an aid to Clinical burn wound management specifically, rather than for research. The official indication for use is to assess the blood flow in burn wounds of the skin, when cleaned of surface debris, to aid in the Clinician’s assessment of burn wound healing potential.

The new system offers very rapid scanning of smaller areas ideally suited to scenarios when time is tight.

If you would like to read more about this or find out about arranging a no obligation evaluation in your unit, please contact us directly and we will be happy to help.