510(k) Report

FDA applicant

Sorbx, LLC

Ponte Vedra Beach, FL1 decision2007–20070 recalls

FDA records 1 decision for Sorbx, LLC (Ponte Vedra Beach, FL) in 2007: 1 510(k) clearance. All are in product code GDW (Staple, Implantable). 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 Sorbx, LLC’s devices, and how often a recall has named them.

FDA decisions per year

1in 2007

2007: 1
2007high 1 (2007) · low 0 (2008)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Sorbx, LLC by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • GDWStaple, Implantable1decision

Who builds on its devices?

Later devices cite its devices 2 times; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K071061Absorbatack and ApplicatorSorbx, LLC · 20072cite it

What has FDA decided for it lately?

  • K071061Absorbatack and ApplicatorSorbx, LLC · 2007

The one decision as Sorbx, LLC →