510(k) Report

FDA applicant

Santec Corporation

Komaki, JP2 decisions2015–20190 recalls

FDA records 2 decisions for Santec Corporation (Komaki, JP) from 2015 to 2019: 2 510(k) clearances. All are in product code MXK (Device, Analysis, Anterior Segment). 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, ophthalmic panel, where it files most

How often FDA has decided Santec Corporation’s devices, and how often a recall has named them.

FDA decisions per year

1in 2019

2015: 12019: 1
2015high 1 (2015) · low 0 (2016)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2015.

FIG. 1 — Santec Corporation by year, 2015–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • MXKDevice, Analysis, Anterior Segment2decisions

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.

  • K150754ARGOSSantec Corporation · 20151cites it

What has FDA decided for it lately?

  • K191051ARGOSSantec Corporation · 2019
  • K150754ARGOSSantec Corporation · 2015

All 2 as Santec Corporation →