510(k) Report

FDA applicant

Trans-Atlantic Dental

Trenton, NJ1 decision1999–19990 recalls

FDA records 1 decision for Trans-Atlantic Dental (Trenton, NJ) in 1999: 1 510(k) clearance. All are in product code EBI (Resin, Denture, Relining, Repairing, Rebasing). 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, dental panel, where it files most

How often FDA has decided Trans-Atlantic Dental’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Trans-Atlantic Dental since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Trans-Atlantic Dental 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?

  • EBIResin, Denture, Relining, Repairing, Rebasing1decision

What has FDA decided for it lately?

  • K983461Uni-Flex ResinTrans-Atlantic Dental · 1999

The one decision as Trans-Atlantic Dental →

Other applicant names beginning “Trans-Atlantic”

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 Pace, Inc. 1