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Data / Medical devices / Apparatus, Vestibular Analysis / United States

FDA-registered makers of Apparatus, Vestibular Analysis in the United States: 6 establishments

6 establishments in the United States are registered with the FDA to make Apparatus, Vestibular Analysis (product code LXV). 5 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.

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Device
Apparatus, Vestibular Analysis
Product code
LXV
Country
United States

Makers of Apparatus, Vestibular Analysis in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Diversified Healthcare Development LLC.Independence, VA, United StatesManufacturer2April 18, 2007000api.fda.gov
King-Devick Technologies, IncOak Brook, IL, United StatesManufacturer1April 2, 2018000api.fda.gov
Sway Medical, Inc.Tulsa, OK, United StatesManufacturer1September 20, 2012000api.fda.gov
Ultrathera Technologies, Inc.Colorado Springs, CO, United StatesManufacturer1April 27, 2022000api.fda.gov
Upright Science, Inc.Palm Bch Gdns, FL, United StatesManufacturer1August 16, 2019000api.fda.gov
R and D Engineering Inc of EarlhamEarlham, IA, United StatesContract manufacturer0000api.fda.gov

Updated November 2, 2026. 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.