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Laser vaginal rejuvenation devices cancelled from ARTG

17 Mar 2025

Karen Stephens

by Karen Stephens

Female doctor with worried looking female patient

Energy-based devices for vaginal rejuvenation were cancelled from the Australian Register of Therapeutic Goods (ARTG) in February 2025. There are currently no devices included in the ARTG that are approved for use for vaginal rejuvenation. Devices already in use can continue to be used, however your professional indemnity policy may not cover them. Devices used for other purposes such as dermatology are still on the ARTG.

The decision was made following a TGA review which found there was insufficient clinical evidence to support the therapeutic use and long-term safety of these devices.

‘Energy-based’ means these devices use laser energy, including radiofrequency (RF), carbon dioxide (CO2), or Er:YAG (erbium-doped yttrium aluminium garnet) lasers.

For guidance on alternative treatments see:

ARTG status of particular devices can be found here.

 

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This blog contains general information only. We recommend you contact your medical defence organisation or insurer when you require specific advice in relation to medico-legal matters. The MDA National Group is made up of MDA National Limited ABN 67 055 801 771 and MDA National Insurance Pty Ltd ABN 56 058 271 417 AFS Licence No. 238073.

 

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