510(k) Report

FDA applicant

Upright Science, Inc.

Palm Beach Gardens, FL1 decision2019–20190 recalls

FDA records 1 decision for Upright Science, Inc. (Palm Beach Gardens, FL) in 2019: 1 510(k) clearance. All are in product code LXV (Apparatus, Vestibular Analysis). Its devices cite 1 predicate, 0 of them its own earlier devices. No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

How often FDA has decided Upright Science, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2019

2019: 1
2019high 1 (2019) · low 0 (2020)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2019.

FIG. 1 — Upright Science, Inc. by year, 2019–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Upright Science, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Which product codes does it file in?

  • LXVApparatus, Vestibular Analysis1decision

Whose devices does it build on?

Its devices cite 1 predicate; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K190735EQ BalanceUpright Science, Inc. · 2019

The one decision as Upright Science, Inc. →