MADE IN THE USA
LightScalpel Inc is proud to announce that this past September of 2019, LightScalpel has successfully completed the Medical Device Single Audit Program (MDSAP) recertification with the addition of Australia requirements, which is ISO’s mandatory process for LightScalpel laser products to become available outside of USA and Canada. LightScalpel is excited to soon bring its proprietary CO2 lasers with exclusive fiber delivery to patients and practitioners in Australia, where the approval from the Australian TGA is pending.
