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Aventamed Dac

Ireland IE-MF-000004115 Last updated 23 Oct 2026

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Devices
3
Registries
EUDAMEDFDA 510(k)GUDIDFDA
FDA recalls
0

Catalogue3

What Aventamed Dac makes

Aventamed Dac manufactures tympanostomy tube devices, including the Solo+ Tympanostomy Tube Device (TTD), Solo+ TTD, and related components such as the Solo+ Tympanostomy Tube Handpiece and Cartridge.

The company's products are classified as Class II and Class IIb medical devices and are listed in the EUDAMED and FDA 510(k) registries. Aventamed Dac is based in Ireland.

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

Frequently asked questions

What medical devices does Aventamed Dac manufacture?

Aventamed Dac manufactures tympanostomy tube devices, including the Solo+ Tympanostomy Tube Device (TTD), Solo+ TTD, and related components such as the Solo+ Tympanostomy Tube Handpiece and Cartridge.

Where is Aventamed Dac based?

Aventamed Dac is based in Ireland, as indicated in the device registry information.

Which regulatory registries list Aventamed Dac's devices?

Aventamed Dac's devices are listed in the EUDAMED and FDA 510(k) registries, which are regulatory databases for medical devices in the European Union and United States respectively.

How are Aventamed Dac's devices classified?

Aventamed Dac's devices are classified as Class II and Class IIb medical devices, which indicates their level of risk and the regulatory controls they require.

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

Information

Country
Ireland
Address
Rubicon Centre, Rossa Avenue, Cork, Ireland
Phone
+353 21 492 8980
PRRC contact
John Vaughan
EUDAMED SRN
IE-MF-000004115
FDA FEI number
3012112259