510(k) Report

FDA applicant

Pfrimmer-Viggo GmbH & Co.

Washington, DC1 decision1992–19920 recalls

FDA records 1 decision for Pfrimmer-Viggo GmbH & Co. (Washington, DC) in 1992: 1 510(k) clearance. All are in product code LEM (Human Lyophilized Dura Mater). 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, neurology panel, where it files most

How often FDA has decided Pfrimmer-Viggo GmbH & Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Pfrimmer-Viggo GmbH & Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Pfrimmer-Viggo GmbH & Co. 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?

  • LEMHuman Lyophilized Dura Mater1decision

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.

  • K910555Tutoplast DuraPfrimmer-Viggo GmbH & Co. · 19922cite it

What has FDA decided for it lately?

  • K910555Tutoplast DuraPfrimmer-Viggo GmbH & Co. · 1992

The one decision as Pfrimmer-Viggo GmbH & Co. →