510(k) Report

FDA applicant

Shenzhen Ruiyi Business Technology Co., Ltd.

Shenzhen, CN2 decisions2022–20240 recalls

FDA records 2 decisions for Shenzhen Ruiyi Business Technology Co., Ltd. (Shenzhen, CN) from 2022 to 2024: 2 510(k) clearances. All are in product code IRP (Massager, Powered Inflatable Tube). Its devices cite 3 predicates, 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

FIG. A — Illustration, physical medicine panel, where it files most

How often FDA has decided Shenzhen Ruiyi Business Technology Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2024

2022: 12024: 1
2022high 1 (2022) · low 0 (2023)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2022.

FIG. 1 — Shenzhen Ruiyi Business Technology Co., Ltd. by year, 2022–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • IRPMassager, Powered Inflatable Tube2decisions

Whose devices does it build on?

Its devices cite 3 predicates; 0 are its own earlier devices. The firms it cites most:

Who builds on its devices?

Later devices cite its devices 2 times; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K232965Leg Massager (Models:RP-ALM070H, RP-ALM071H)Shenzhen Ruiyi Business Technology Co., Ltd. · 20242cite it

What has FDA decided for it lately?

  • K232965Leg Massager (Models:RP-ALM070H, RP-ALM071H)Shenzhen Ruiyi Business Technology Co., Ltd. · 2024
  • K222924Leg Massager RF-ALM070Shenzhen Ruiyi Business Technology Co., Ltd. · 2022

All 2 as Shenzhen Ruiyi Business Technology Co., Ltd. →