510(k) Report

FDA applicant

Arrive Systems, Inc.

New Ark, DE1 decision2021–20210 recalls

FDA records 1 decision for Arrive Systems, Inc. (New Ark, DE) in 2021: 1 510(k) clearance. All are in product code NGX (Stimulator, Muscle, Powered, For Muscle…). 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, physical medicine panel, where it files most

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

FDA decisions per year

1in 2021

2021: 1
2021high 1 (2021) · low 0 (2022)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2021.

FIG. 1 — Arrive Systems, Inc. by year, 2021–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Arrive Systems, 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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