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Building on our long history and heritage in the field of orthopaedic medical devices, LockDown has been delivering excellent outcomes in soft tissue reconstruction for more than 15 years.
Many thousands of devices have been used in acromioclavcular reconstruction over more than 15 years all over the world. This weight of clinical evidence combined with exceptional patient approval means LockDown should be the technique of choice.
LockDown are committed to providing educational content around our products. The weight of clinical evidence, both born out of and supplemented by our relationships with key opinion leaders around the world is presented here along with clinical presentations and (for Medical Professionals) videos revealing the nuances around our surgical techniques.
“LockDown™ was first introduced as a method of addressing failed ACJ surgery and this was how I was introduced to the technique. It has since gained popularity as a primary method of stabilizing the disrupted ACJ and I have routinely used it as my first choice for ACJ reconstruction for over 6 years.”
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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