510(k) Report

FDA applicant

Seedings Life Science Ventures, LLC

New York, NY2 decisions2013–20140 recalls

FDA records 2 decisions for Seedings Life Science Ventures, LLC (New York, NY) from 2013 to 2014: 2 510(k) clearances. All are in product code EZL (Catheter, Retention Type, Balloon). 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, gastroenterology and urology panel, where it files most

How often FDA has decided Seedings Life Science Ventures, LLC’s devices, and how often a recall has named them.

FDA decisions per year

1in 2014

2013: 12014: 1
2013high 1 (2013) · low 0 (2015)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2013.

FIG. 1 — Seedings Life Science Ventures, LLC by year, 2013–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Seedings Life Science Ventures, LLC’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Which product codes does it file in?

  • EZLCatheter, Retention Type, Balloon2decisions

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.

  • K131655Lighthouse (TM) Urinary CatheterSeedings Life Science Ventures, LLC · 20131cites it

What has FDA decided for it lately?

  • K140099Lighthouse Urinary CatheterSeedings Life Science Ventures, LLC · 2014
  • K131655Lighthouse (TM) Urinary CatheterSeedings Life Science Ventures, LLC · 2013

All 2 as Seedings Life Science Ventures, LLC →