510(k) Report

FDA applicant

Trans Pace, Inc.

Mchenry, IL1 decision1982–19820 recalls

FDA records 1 decision for Trans Pace, Inc. (Mchenry, IL) in 1982: 1 510(k) clearance. All are in product code LDF (Electrode, Pacemaker, Temporary). 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, cardiovascular panel, where it files most

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

FDA decisions per year

No FDA decision for Trans Pace, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Trans Pace, Inc. 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?

  • LDFElectrode, Pacemaker, Temporary1decision

What has FDA decided for it lately?

  • K820232Transthoracic Temp. Pacemaker #100TPETrans Pace, Inc. · 1982

The one decision as Trans Pace, Inc. →

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 Texas Medical Devices Corp. 1Trans-America Enterprises Corp. 1Trans-Med Corp. 1Trans American Chemical Corp. 1Trans-Pacific Healthcare-USA 1Trans Aire 1Trans Ancient Products Co., Ltd. 1Trans-Atlantic Dental 1