Data / Medical devices / United States / Addivation Medical

Addivation Medical: FDA-registered device maker in Reno, NV, United States, 1 510(k) clearance

Addivation Medical is registered with the FDA (registration 3023434937) in Reno, NV, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated July 30, 2019. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number

3023434937

Address

770 Smithridge Dr Ste 700, Reno, NV, United States, 89502

Owner or operator

Addivation Medical LLC (10085737)

Roles

Specification developer

First device listed

February 13, 2023

Registered through

2026

Brand names listed

Addivation Medical Cervical Interbody Device

Devices it lists

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.

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Updated July 30, 2019. 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.