510(k) Report

FDA applicant

Knight Medical, Inc.

Houston, TX5 decisions1986–19930 recalls

FDA records 5 decisions for Knight Medical, Inc. (Houston, TX) from 1986 to 1993: 5 510(k) clearances. Most are in product codes KNT (Tubes, Gastrointestinal (And Accessories)) and FCN (Urinary Drainage Collection Kit, For…). 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, gastroenterology and urology panel, where it files most

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

FDA decisions per year

No FDA decision for Knight Medical, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Knight Medical, 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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