510(k) Report

FDA applicant

D & D Holdings, LLC

Nashville, TN1 decision2006–20060 recalls

FDA records 1 decision for D & D Holdings, LLC (Nashville, TN) in 2006: 1 510(k) clearance. All are in product code KMF (Bandage, Liquid). 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 D & D Holdings, LLC’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for D & D Holdings, LLC since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — D & D Holdings, LLC 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?

  • KMFBandage, Liquid1decision

Whose devices does it build on?

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

What has FDA decided for it lately?

  • K042955Cuticover Skin Barrier DeviceD & D Holdings, LLC · 2006

The one decision as D & D Holdings, LLC →