510(k) Report

FDA applicant

Dexide, Inc.

Fort Worth, TX38 decisions1978–19990 recalls

FDA records 38 decisions for Dexide, Inc. (Fort Worth, TX) from 1978 to 1999: 38 510(k) clearances. Most are in product codes GCJ (Laparoscope, General & Plastic Surgery) and GEC (Brush, Scrub, Operating-Room). Its devices cite 5 predicates, 3 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 and plastic surgery panel, where it files most

How often FDA has decided Dexide, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dexide, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Dexide, 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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