510(k) Report

FDA applicant

Ad Rem Technology Sarl

Potomac, MD2 decisions2008–20150 recalls

FDA records 2 decisions for Ad Rem Technology Sarl (Potomac, MD) from 2008 to 2015: 2 510(k) clearances. Most are in product codes NGX (Stimulator, Muscle, Powered, For Muscle…) and IPF (Stimulator, Muscle, Powered). Its devices cite 3 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 Ad Rem Technology Sarl’s devices, and how often a recall has named them.

FDA decisions per year

1in 2015

2008: 12015: 1
2008high 1 (2008) · low 0 (2009)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2008.

FIG. 1 — Ad Rem Technology Sarl by year, 2008–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Ad Rem Technology Sarl’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?

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

Whose devices does it build on?

Its devices cite 3 predicates; 1 are its own earlier devices. The firms it cites most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K072252Veinoplus Neuromuscular StimulatorAd Rem Technology Sarl · 20081cites it

What has FDA decided for it lately?

  • K141919Veinoplus Sport Neuromuscular StimulatorAd Rem Technology Sarl · 2015
  • K072252Veinoplus Neuromuscular StimulatorAd Rem Technology Sarl · 2008

All 2 as Ad Rem Technology Sarl →