510(k) Report

FDA applicant

Endovascular, Inc.

Costa Mesa, CA3 decisions1993–19930 recalls

FDA records 3 decisions for Endovascular, Inc. (Costa Mesa, CA) in 1993: 3 510(k) clearances. Most are in product codes LYK (Angioscope) and MGZ (Valvulotome). 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 Endovascular, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Endovascular, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Endovascular, 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?

  • LYKAngioscope2decisions
  • MGZValvulotome1decision

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.

  • K923996Disposable Vascular AngioscopeEndovascular, Inc. · 19931cites it

What has FDA decided for it lately?

  • K931421Disposable Steerable AngioscopeEndovascular, Inc. · 1993
  • K924075Disposable Optical ValvulotomeEndovascular, Inc. · 1993
  • K923996Disposable Vascular AngioscopeEndovascular, Inc. · 1993

All 3 as Endovascular, Inc. →

Other applicant names beginning “Endovascular”

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

Endovascular Engineering 4Endovascular Instruments, Inc. 1