Data / Medical devices / United States / Xironetic R&D Center

Xironetic R&D Center: FDA-registered device maker in Oklahoma City, OK, United States, 1 510(k) clearance

Xironetic R&D Center is registered with the FDA (registration 3027408258) in Oklahoma City, OK, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated October 21, 2022. Registered through 2026. FDA data exported November 3, 2026.

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FDA registration number

3027408258

Address

201 Robert S Kerr Ave Ste 257, Oklahoma City, OK, United States, 73102

Owner or operator

Xironetic (10088189)

Roles

Manufacturer

First device listed

June 7, 2023

Registered through

2026

Brand names listed

IntraOpVSP

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 October 21, 2022. 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.