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Find information for planning your business project.

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Queensland Cosmetic Lasers: Check Three Licence Stages

Queensland Health lists possession, approval-to-acquire and use licences for cosmetic laser businesses. Plan those steps before ordering equipment.

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Australia Light-Based Treatments: Plan Client Screening

ARPANSA's provider advice helps Australian laser, IPL and LED operators build a consultation and incident-response process before offering treatments.

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Australia: When a Beauty Light Device Needs TGA Review

TGA guidance draws a product-claim boundary for radiating beauty equipment. Australian buyers should verify intended use before importing or advertising.

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EU Aesthetic-Device CE Files: Check the Notified Body

For EU aesthetic-equipment procurement, a CE logo alone is not enough: check whether a notified body is required and whether its designation covers the device.

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EU Annex XVI: Which Aesthetic Light Devices Are In Scope?

EU MDCG guidance shows why buyers must check a light device's intended purpose and intensity before assuming Annex XVI covers, or excludes, the product.

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UK Hair-Removal Advertising: Test Every IPL Claim

UK CAP advice on hair-removal advertising shows why IPL sellers should distinguish reduction from permanence and substantiate comfort and efficacy claims.

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UK Laser and IPL Rooms: Turn MHRA Guidance Into Checks

The MHRA's laser, IPL and LED guidance gives UK operators a framework for room controls, staff roles and equipment checks before offering a service.

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US Medical Lasers: A Procurement File Beyond the Brochure

FDA's medical-laser overview separates radiation-product duties from medical-device rules. Use both perspectives when checking a US cosmetic-laser purchase.

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US Light-Device Claims: What Evidence Should Buyers Request?

FTC guidance helps US buyers test claims about light-based aesthetic devices: identify the promised outcome, request relevant evidence and check its limits.

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US Aesthetic Device Buying: Verify FDA Status, Not a Certificate

A buyer's practical check for US aesthetic-device listings: distinguish FDA registration from clearance or approval and verify the exact model and intended use.

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