510(k) Report

FDA applicant

Bomei Co, Ltd.

Taoyuan City, TW2 decisions2016–20210 recalls

FDA records 2 decisions for Bomei Co, Ltd. (Taoyuan City, TW) from 2016 to 2021: 2 510(k) clearances. All are in product code OAT (Implant, Endosseous, Orthodontic). Its devices cite 2 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, dental panel, where it files most

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

FDA decisions per year

1in 2021

2016: 12021: 1
2016high 1 (2016) · low 0 (2017)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2016.

FIG. 1 — Bomei Co, Ltd. by year, 2016–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • OATImplant, Endosseous, Orthodontic2decisions

Whose devices does it build on?

Its devices cite 2 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.

  • K152297OBS Anchorage ScrewBomei Co, Ltd. · 20161cites it

What has FDA decided for it lately?

  • K202278OBS Anchorage Screw, Biokey Anchorage ScrewBomei Co, Ltd. · 2021
  • K152297OBS Anchorage ScrewBomei Co, Ltd. · 2016

All 2 as Bomei Co, Ltd. →