510(k) Report

FDA applicant

Axiom Technology Partners, LLC

Belmont, CA1 decision2010–20100 recalls

FDA records 1 decision for Axiom Technology Partners, LLC (Belmont, CA) in 2010: 1 510(k) clearance. All are in product code OCW (Endoscopic Tissue Approximation Device). 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 Axiom Technology Partners, LLC’s devices, and how often a recall has named them.

FDA decisions per year

1in 2010

2010: 1
2010high 1 (2010) · low 0 (2011)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2010.

FIG. 1 — Axiom Technology Partners, LLC by year, 2010–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • OCWEndoscopic Tissue Approximation Device1decision

Who builds on its devices?

Later devices cite its devices 1 time; 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.

  • K103412Axiom Fascial Closure SystemAxiom Technology Partners, LLC · 20101cites it

What has FDA decided for it lately?

  • K103412Axiom Fascial Closure SystemAxiom Technology Partners, LLC · 2010

The one decision as Axiom Technology Partners, LLC →

Other applicant names beginning “Axiom”

FDA records each applicant name separately; these may or may not be the same firm.

Axiom Medical, Inc. 28Axiom Worldwide, Inc. 4Axiom, Inc. 4Axiom Usa., Inc. 4Axiom Manufacturing 2Axiom Orthopaedics, Inc. 1Axiom Ent. Co., Ltd. 1