510(k) Report

FDA applicant

Capital Marketing Technologies, Inc.

Waco, TX2 decisions1999–19990 recalls

FDA records 2 decisions for Capital Marketing Technologies, Inc. (Waco, TX) in 1999: 2 510(k) clearances. All are in product code MDA (Elastomer, Silicone, For Scar Management). 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 Capital Marketing Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Capital Marketing Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Capital Marketing Technologies, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Capital Marketing Technologies, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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