510(k) Report

FDA applicant

Ti-Mesh, Inc.

Las Vegas, NV3 decisions1992–19930 recalls

FDA records 3 decisions for Ti-Mesh, Inc. (Las Vegas, NV) from 1992 to 1993: 3 510(k) clearances. Most are in product codes JEY (Plate, Bone) and FTM (Mesh, Surgical). 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, dental panel, where it files most

How often FDA has decided Ti-Mesh, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ti-Mesh, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Ti-Mesh, Inc. 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?

  • JEYPlate, Bone2decisions
  • FTMMesh, Surgical1decision

Who builds on its devices?

Later devices cite its devices 11 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.

  • K923419Tismesh SystemTi-Mesh, Inc. · 19936cite it
  • K923802Timesh Titanium Mini-Softplate/ScrewTi-Mesh, Inc. · 19924cite it
  • K922308Tilghman Titanium Mesh Skeletal Orbit LinerTi-Mesh, Inc. · 19931cites it

What has FDA decided for it lately?

  • K923419Tismesh SystemTi-Mesh, Inc. · 1993
  • K922308Tilghman Titanium Mesh Skeletal Orbit LinerTi-Mesh, Inc. · 1993
  • K923802Timesh Titanium Mini-Softplate/ScrewTi-Mesh, Inc. · 1992

All 3 as Ti-Mesh, Inc. →