510(k) Report

FDA applicant

Dura-Vac Products

Ventura, CA1 decision1996–19960 recalls

FDA records 1 decision for Dura-Vac Products (Ventura, CA) in 1996: 1 510(k) clearance. All are in product code MMK (Container, Sharps). Its devices cite 1 predicate, 0 of them its own earlier devices. 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 hospital panel, where it files most

How often FDA has decided Dura-Vac Products’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dura-Vac Products since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Dura-Vac Products 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?

  • MMKContainer, Sharps1decision

Whose devices does it build on?

Its devices cite 1 predicate; 0 are its own earlier devices. The firms it cites most:

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.

  • K955514Sharps Safe 1.5 & Sharps Safe 2.0Dura-Vac Products · 19962cite it

What has FDA decided for it lately?

  • K955514Sharps Safe 1.5 & Sharps Safe 2.0Dura-Vac Products · 1996

The one decision as Dura-Vac Products →

Other applicant names beginning “Dura-Vac”

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

Dura Pharmaceuticals, Inc. 3Dura Tap, LLC 2Dura Corp., The 1