510(k) Report

FDA applicant

D.T. Davis Enterprises Ltd. T/A Hovertech Int'L

Bethlehem, PA2 decisions2010–20120 recalls

FDA records 2 decisions for D.T. Davis Enterprises Ltd. T/A Hovertech Int'L (Bethlehem, PA) from 2010 to 2012: 2 510(k) clearances. Most are in product codes INK (Stretcher, Wheeled, Powered) and FNG (Lift, Patient, Ac-Powered). Its devices cite 1 predicate, 0 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 D.T. Davis Enterprises Ltd. T/A Hovertech Int'L’s devices, and how often a recall has named them.

FDA decisions per year

1in 2012

2010: 12012: 1
2010high 1 (2010) · low 0 (2011)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2010.

FIG. 1 — D.T. Davis Enterprises Ltd. T/A Hovertech Int'L by year, 2010–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • INKStretcher, Wheeled, Powered1decision
  • FNGLift, Patient, Ac-Powered1decision

Whose devices does it build on?

Its devices cite 1 predicate; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K121287HT-WedgeD.T. Davis Enterprises Ltd. T/A Hovertech Int'L · 2012
  • K102236Hovertrans Transformer with Power Drive Model HTT-650PD.T. Davis Enterprises Ltd. T/A Hovertech Int'L · 2010

All 2 as D.T. Davis Enterprises Ltd. T/A Hovertech Int'L →