FDA applicant

Ness-Neuromuscular Electrical Stimulation Systems

Washington, DC7 decisions2001–20110 recalls

FDA records 7 decisions for Ness-Neuromuscular Electrical Stimulation Systems (Washington, DC) from 2001 to 2011: 7 510(k) clearances. Most are in product codes GZI (Stimulator, Neuromuscular, External Functional) and IPG (Shoe, Cast). Its devices cite 13 predicates, 2 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, neurology panel, where it files most

How often FDA has decided Ness-Neuromuscular Electrical Stimulation Systems’s devices, and how often a recall has named them.

FDA decisions per year

1in 2011

2007high 1 (2008) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Ness-Neuromuscular Electrical Stimulation Systems by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Ness-Neuromuscular Electrical…’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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Other applicant names beginning “Ness-Neuromuscular”

FDA records each applicant name separately; these may or may not be the same firm.

N.E.S.S. Nuromuscular Electrical Stimulation Syst 1

Ness-Neuromuscular Electrical Stimulation Systems

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Ness-Neuromuscular”