510(k) Report

FDA applicant

Lv Liberty Vision Corporation

Portsmouth, NH2 decisions2017–20200 recalls

FDA records 2 decisions for Lv Liberty Vision Corporation (Portsmouth, NH) from 2017 to 2020: 2 510(k) clearances. All are in product code KXK (Source, Brachytherapy, Radionuclide). Its devices cite 2 predicates, 1 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Lv Liberty Vision Corp.”.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, radiology panel, where it files most

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

FDA decisions per year

1in 2020

2017: 12020: 1
2017high 1 (2017) · low 0 (2018)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2017.

FIG. 1 — Lv Liberty Vision Corporation by year, 2017–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • KXKSource, Brachytherapy, Radionuclide2decisions

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.

  • K163572LV Liberty Vision Model 1 90 Yttrium Brachytherapy SourceLv Liberty Vision Corp. · 20171cites it

What has FDA decided for it lately?

  • K193602LV Liberty Vision Model 1 90Yttrium Brachytherapy SourceLv Liberty Vision Corporation · 2020
  • K163572LV Liberty Vision Model 1 90 Yttrium Brachytherapy SourceLv Liberty Vision Corp. · 2017

The one decision as Lv Liberty Vision Corporation →The one decision as Lv Liberty Vision Corp. →