510(k) Report

FDA applicant

Arp Manufacturing, Inc.

Boulder, CO2 decisions2009–20100 recalls

FDA records 2 decisions for Arp Manufacturing, Inc. (Boulder, CO) from 2009 to 2010: 2 510(k) clearances. Most are in product codes IPF (Stimulator, Muscle, Powered) and NGX (Stimulator, Muscle, Powered, For Muscle…). Its devices cite 4 predicates, 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 Arp Manufacturing, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2010

2009: 12010: 1
2009high 1 (2009) · low 0 (2011)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2009.

FIG. 1 — Arp Manufacturing, Inc. by year, 2009–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Arp Manufacturing, 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?

  • IPFStimulator, Muscle, Powered1decision
  • NGXStimulator, Muscle, Powered, For Muscle Conditioning1decision

Whose devices does it build on?

Its devices cite 4 predicates; 0 are its own earlier devices. The firms it cites most:

Who builds on its devices?

Later devices cite its devices 1 time; 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.

  • K093999Arp Pov SportArp Manufacturing, Inc. · 20101cites it

What has FDA decided for it lately?

  • K093999Arp Pov SportArp Manufacturing, Inc. · 2010
  • K093259ARP RX100Arp Manufacturing, Inc. · 2009

All 2 as Arp Manufacturing, Inc. →