510(k) Report

FDA applicant

Vesocclude Medical, LLC

Spring Hope, NC2 decisions2009–20160 recalls

FDA records 2 decisions for Vesocclude Medical, LLC (Spring Hope, NC) from 2009 to 2016: 2 510(k) clearances. All are in product code FZP (Clip, Implantable). Its devices cite 9 predicates, 0 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 Vesocclude Medical, LLC’s devices, and how often a recall has named them.

FDA decisions per year

1in 2016

2009: 12016: 1
2009high 1 (2009) · low 0 (2010)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2009.

FIG. 1 — Vesocclude Medical, LLC by year, 2009–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Vesocclude Medical, 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?

  • FZPClip, Implantable2decisions

Whose devices does it build on?

Its devices cite 9 predicates; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K152082Vesocclude Polymer Ligating ClipVesocclude Medical, LLC · 2016
  • K091060Vesocclude Ligating ClipVesocclude Medical, LLC · 2009

All 2 as Vesocclude Medical, LLC →