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Wallaby Medical

United States US-MF-000010241 Last updated 25 Oct 2026

Devices
257
Registries
EUDAMEDFDA
FDA recalls
0

Catalogue257

Page 1 of 6

Showing 1-50 of 257

EUDAMED certificates1

Held under this manufacturer's EUDAMED registration, grouped by notified body; in force first, then by expiry.

EUDAMED certificates (1)

Notified body 2797 1 certificate

  • MDR 807342 Supplemented

    Technical documentation EU MDR

    Issued
    20 Aug 2026
    Expires
    22 Jul 2030
    Reason
    Change approved

Authorised representatives

Notified bodies

  • Notified body 2797

What Wallaby Medical makes

Wallaby Medical manufactures the Wallaby Avenir™ Coil System, a medical device used for vascular embolization procedures.

The Wallaby Avenir™ Coil System is classified as Class II and Class III and is listed in the EUDAMED and FDA 510(k) registries. Wallaby Medical is 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 does Wallaby Medical make?

Wallaby Medical manufactures the Wallaby Avenir™ Coil System, a medical device used for vascular embolization procedures, as stated in the provided summary.

Where is Wallaby Medical based?

Wallaby Medical is based in the United States, as explicitly mentioned in the summary section of the device data.

Which registries list Wallaby Medical's devices?

Wallaby Medical's devices are listed in the EUDAMED and FDA 510(k) registries, as specified in the LISTED IN field of the device data.

How are Wallaby Medical's devices classified?

Wallaby Medical's devices are classified as Class II and Class III, as indicated in the DEVICE CLASSES field of the provided data.

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

Information

Country
United States
Address
22901, Mill Creek Drive, Laguna Hills, United States
Phone
+1 858.437.2286
PRRC contact
Nathaniel Knock
EUDAMED SRN
US-MF-000010241
FDA FEI number
3012543881