FDA applicant

Vr Vertical, LLC Dba Xrgo

Louisville, KY1 decision2021–20210 recalls

FDA records 1 decision for Vr Vertical, LLC Dba Xrgo (Louisville, KY) in 2021: 1 510(k) clearance. All are in product code FXX (Mask, Surgical). No recall is linked to its devices.

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

FIG. A — Illustration, general and plastic surgery panel, where it files most

How often FDA has decided Vr Vertical, LLC Dba Xrgo’s devices, and how often a recall has named them.

FDA decisions per year

1in 2021

2021high 1 (2021) · low 0 (2022)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2021.

FIG. 1 — Vr Vertical, LLC Dba Xrgo by year, 2021–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Vr Vertical, LLC Dba Xrgo’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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Vr Vertical, LLC Dba Xrgo

Which product codes does it file in?

What has FDA decided for it lately?