FDA applicant

Phx Technologies Corp.

Lewisville, TX49 decisions1993–19980 recalls

FDA records 49 decisions for Phx Technologies Corp. (Lewisville, TX) from 1993 to 1998: 49 510(k) clearances. Most are in product codes GCJ (Laparoscope, General & Plastic Surgery) and HRX (Arthroscope). 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 Phx Technologies Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Phx Technologies Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Phx Technologies Corp.

Which product codes does it file in?

What has FDA decided for it lately?