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Aeon Astron Europe B.V.

NL Last updated 22 Oct 2026

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Devices
3
Registries
FDA 510(k)
FDA recalls
0

Catalogue3

What Aeon Astron Europe B.V. makes

Aeon Astron Europe B.V. manufactures collagen matrix products, including the ologen Collagen Matrix, AONGEN Collagen Matrix, and AONGEN Dental Collagen Matrix.

These devices are classified as Class U and are listed in the FDA 510(k) registry, with the company based in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Aeon Astron Europe B.V. manufacture?

Aeon Astron Europe B.V. specializes in the production of collagen matrix products. Their current product portfolio includes the ologen Collagen Matrix, the AONGEN Collagen Matrix, and the AONGEN Dental Collagen Matrix, which are designed for specific clinical applications.

Where is Aeon Astron Europe B.V. based?

Aeon Astron Europe B.V. is based in the United States. This location serves as the primary operational base for the company's manufacturing and regulatory activities regarding their collagen matrix product line.

How are the devices from Aeon Astron Europe B.V. classified and registered?

The collagen matrix devices manufactured by Aeon Astron Europe B.V. are classified as Class U. These specific devices are listed within the FDA 510(k) registry, which is the regulatory pathway used to document that these products have been reviewed for market entry.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
NL