510(k) Report

FDA applicant

Vat-Tech, Inc.

Palm Harbor, FL2 decisions1989–19960 recalls

FDA records 2 decisions for Vat-Tech, Inc. (Palm Harbor, FL) from 1989 to 1996: 2 510(k) clearances. All are in product code ITH (Equipment, Traction, Powered). Its devices cite 1 predicate, 1 of them its own earlier devices. 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, physical medicine panel, where it files most

How often FDA has decided Vat-Tech, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Vat-Tech, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Vat-Tech, 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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Which product codes does it file in?

  • ITHEquipment, Traction, Powered2decisions

Who builds on its devices?

Later devices cite its devices 9 times; 1 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K951622Vax-D Therapeutic TableVat-Tech, Inc. · 19968cite it
  • K894435Vax-T Pelvic Traction BeltVat-Tech, Inc. · 19891cites it

What has FDA decided for it lately?

  • K951622Vax-D Therapeutic TableVat-Tech, Inc. · 1996
  • K894435Vax-T Pelvic Traction BeltVat-Tech, Inc. · 1989

All 2 as Vat-Tech, Inc. →