510(k) Report

FDA applicant

Shenzhen Mywin Technology Co., Ltd.

Shenzhen, CN2 decisions2021–20220 recalls

FDA records 2 decisions for Shenzhen Mywin Technology Co., Ltd. (Shenzhen, CN) from 2021 to 2022: 2 510(k) clearances. Most are in product codes ONF (Powered Light Based Non-Laser Surgical…) and OHT (Light Based Over-The-Counter Hair Removal). Its devices cite 4 predicates, 1 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, general and plastic surgery panel, where it files most

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

FDA decisions per year

1in 2022

2021: 12022: 1
2021high 1 (2021) · low 0 (2023)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2021.

FIG. 1 — Shenzhen Mywin Technology Co., Ltd. by year, 2021–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • ONFPowered Light Based Non-Laser Surgical Instrument With Thermal Effect1decision
  • OHTLight Based Over-The-Counter Hair Removal1decision

Whose devices does it build on?

Its devices cite 4 predicates; 1 are its own earlier devices. The firms it cites most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K211368IPL Hair Remover, Model: G993, G996, G998 and G885Shenzhen Mywin Technology Co., Ltd. · 20211cites it

What has FDA decided for it lately?

  • K221679IPL Hair Remover, Model: G993, G996, G998 and G885Shenzhen Mywin Technology Co., Ltd. · 2022
  • K211368IPL Hair Remover, Model: G993, G996, G998 and G885Shenzhen Mywin Technology Co., Ltd. · 2021

All 2 as Shenzhen Mywin Technology Co., Ltd. →