510(k) Report

FDA applicant

Innovative Products, Inc.

Mchenry, IL3 decisions1979–20070 recalls

FDA records 3 decisions for Innovative Products, Inc. (Mchenry, IL) from 1979 to 2007: 3 510(k) clearances. Most are in product codes ION (Exerciser, Non-Measuring) and IPL (Wheelchair, Standup). 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 Innovative Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2007

2007: 1
2007high 1 (2007) · low 0 (2008)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Innovative Products, 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?

  • IONExerciser, Non-Measuring1decision
  • IPLWheelchair, Standup1decision
  • LJLDetectors And Removers, Lice, (Including Combs)1decision

Who builds on its devices?

Later devices cite its devices 3 times; 0 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.

  • K822421Innocomb Lice CombInnovative Products, Inc. · 19822cite it
  • K071390Wheelchair Model STSInnovative Products, Inc. · 20071cites it

What has FDA decided for it lately?

  • K071390Wheelchair Model STSInnovative Products, Inc. · 2007
  • K822421Innocomb Lice CombInnovative Products, Inc. · 1982
  • K790572Lounge, Tilt-a-Body StretchInnovative Products, Inc. · 1979

All 3 as Innovative Products, Inc. →