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Data / Medical devices / New Zealand / Alimetry Ltd

Alimetry Ltd: FDA-registered device maker in Auckland, New Zealand, 2 510(k) clearances

Alimetry Ltd is registered with the FDA (registration 3023209868) in Auckland, New Zealand. It lists 1 device type. The FDA files 2 510(k) clearances under its listings, the newest dated December 5, 2025. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3023209868
Address
86 Symonds St Grafton, Auckland, New Zealand, 1010
Owner or operator
Alimetry Ltd (10085368)
Roles
Complaint file establishment, Manufacturer
First device listed
August 19, 2024
Registered through
2026
Brand names listed
Alimetry Reader, Gastric Alimetry, Gastric Alimetry App, Gastric Alimetry Array, Gastric Alimetry Dock, Gastric Alimetry Kit

Devices it lists

DeviceProduct codeClassRoleSource
System, Electrogastrography (Egg)MYE2Complaint file establishment, Manufactureraccessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
December 5, 2025K252504Gastric AlimetryMYESubstantially EquivalentAlimetry , Ltd.accessdata.fda.gov
July 3, 2024K240946Gastric AlimetryMYESubstantially EquivalentAlimetry , Ltd.accessdata.fda.gov

Compare with other makers

Updated December 5, 2025. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.