510(k) Report

FDA applicant

Lifestand

Houston, TX3 decisions2004–20060 recalls

FDA records 3 decisions for Lifestand (Houston, TX) from 2004 to 2006: 3 510(k) clearances. All are in product code IPL (Wheelchair, Standup). Its devices cite 4 predicates, 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 Lifestand’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Lifestand since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Lifestand’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Which product codes does it file in?

  • IPLWheelchair, Standup3decisions

Whose devices does it build on?

Its devices cite 4 predicates; 1 are its own earlier devices. The firms it cites most:

Who builds on its devices?

Later devices cite its devices 3 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.

  • K041535LSC Lifestand CompactLifestand · 20042cite it
  • K061726LSC, Model 3Lifestand · 20061cites it

What has FDA decided for it lately?

  • K061726LSC, Model 3Lifestand · 2006
  • K042596Lsa HeliumLifestand · 2005
  • K041535LSC Lifestand CompactLifestand · 2004

All 3 as Lifestand →