510(k) Report

FDA applicant

Douglas Bueschel

Santa Barbara, CA1 decision1996–19960 recalls

FDA records 1 decision for Douglas Bueschel (Santa Barbara, CA) in 1996: 1 510(k) clearance. All are in product code FTL (Mesh, Surgical, Polymeric). 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 Douglas Bueschel’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Douglas Bueschel since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Douglas Bueschel 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?

  • FTLMesh, Surgical, Polymeric1decision

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.

  • K963141Kugel Hernia PatchDouglas Bueschel · 19962cite it

What has FDA decided for it lately?

  • K963141Kugel Hernia PatchDouglas Bueschel · 1996

The one decision as Douglas Bueschel →

Other applicant names beginning “Douglas”

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

Douglas Medical Products Corp. 20Douglas James Donaldson Compliance Services 5Douglas Scientific Products 2Douglas C. Yoon, Dds 1Douglas Manufacturer Co. 1Douglas Products 1Douglas C. Mckee & Co. 1