Apolomed
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How are the products certified? Does Apolomed require this in all Devices?

We,Apolomed manufacture equipment srtictly in accordance with ISO 13485 and all our products comply with Medical CE certificates under the Council Directive 93/42/EEC(MDD) and regulations (EU) 2017/745(MDR). Our high end products had obtained certificates of US 510K, Australia TGA, Brazil Anvisa. All the above certificates warrant our Channel Partners to stay relevant in the Global Medical & Aesthetic industries.

Welcome to Apolomed

Choose the site for your region so product availability, documentation, and support information match your location.

  • North America

    Products, education, and regional support for North American practices.

  • All Other Regions

    Products, documentation, and regional support for customers outside North America.