510(k) Report

FDA applicant

Trans Texas Medical Devices Corp.

San Antonio, TX1 decision1983–19830 recalls

FDA records 1 decision for Trans Texas Medical Devices Corp. (San Antonio, TX) in 1983: 1 510(k) clearance. All are in product code LKY (Device, External Penile Rigidity). 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 Trans Texas Medical Devices Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Trans Texas Medical Devices Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Trans Texas Medical Devices Corp. 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?

  • LKYDevice, External Penile Rigidity1decision

What has FDA decided for it lately?

  • K832756Pri a PusTrans Texas Medical Devices Corp. · 1983

The one decision as Trans Texas Medical Devices Corp. →

Other applicant names beginning “Trans”

FDA records each applicant name separately; these may or may not be the same firm.

Trans Vascular Incorporated 2Trans World Agency, Inc. 2Trans-National Trade Development Corp. 2Trans-America Enterprises Corp. 1Trans-Med Corp. 1Trans American Chemical Corp. 1Trans-Pacific Healthcare-USA 1Trans Aire 1Trans Ancient Products Co., Ltd. 1Trans-Atlantic Dental 1Trans Pace, Inc. 1