Our post-market reviews of medical devices supplied in Australia check that devices continue to be safe and perform as expected. We assess that sponsors continue to meet their legal obligations.
A medical device can be selected for post-market review at any time.
Current reviews
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PageFind out more about the post-market review we are undertaking on plastic syringes.
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PageThe TGA is undertaking a post-market review of ventilators included in the Australian Register of Therapeutic Goods.
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PageLearn more about the TGA's post-market review of mercury-containing medical devices.
Completed reviews
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PageFind out more about the post market review we have undertaken on spinal cord stimulators (SCS).
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PageThe TGA has completed a post-market review of all energy-based devices used for vaginal rejuvenation included in the Australian Register of Therapeutic Goods (ARTG).
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PageThe TGA has completed a post-market review of all neonatal incubators included in the Australian Register of Therapeutic Goods (ARTG).
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PageThe Therapeutic Goods Administration (TGA) has undertaken a post-market review of all home-use foetal dopplers included in the Australian Register of Therapeutic Goods (ARTG).
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PageFind out more about the post-market review we have undertaken on human immunodeficiency virus (HIV) nucleic acid tests (NATs).
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PageFind out more about our post-market review on influenza A nucleic acid tests (NATs) and their ability to detect avian influenza A H5N1.
More information
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GuidanceGuidance for sponsors and manufacturers about regulatory requirements for exempt therapeutic goods.
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PageFind out about our process for conducting post-market reviews of medical devices.
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GuidanceGuidance on mandatory requirements and ongoing responsibilities for all manufacturers and sponsors of medical devices.