LASS™ is a simple and reproducible procedure for the reconstruction of medial and lateral ankle ligaments.
It is suitable for both acute and chronic cases and to revise failed previous stabilisation procedures. No specialised instrumentation is required making LASSTM a remarkably straightforward technique. The LASSTM braided device is based on the same technology as the LSSSTM acromioclavicular stabilisation procedure (of which you can discover more here) and so brings the history and clinical heritage of that product into new areas, solving different challenges with a similarly simple and elegant approach.
For more information on the LASSTM technique you can contact us here:
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For more information on the LASS™ technique you can contact us here
We are registered with BSI and hold Certificate no. MD 534510 and operate a Quality Management System which complies with the requirements of ISO 13485:2016.
We are registered with the FDA in the USA, Registration no. 8020712 FEI No. 3008237817.
Our products are CE-marked Certificate No. CE 00403.
Our VAT number is 933 8359 95.
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