FDA applicant

Northeast Orthotics and Prothetics, Inc.

Cranston, RI1 decision2003–20030 recalls

FDA records 1 decision for Northeast Orthotics and Prothetics, Inc. (Cranston, RI) in 2003: 1 510(k) clearance. All are in product code MVA (Orthosis, Cranial). Its devices cite 1 predicate, 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, neurology panel, where it files most

How often FDA has decided Northeast Orthotics and Prothetics, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Northeast Orthotics and Prothetics, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Northeast Orthotics and Prothetics, 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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Other applicant names beginning “Northeast”

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

Northeast Biomedical Labs., Inc. 9 Northeast Scientific, Inc. 6 Northeast Scientific, Inc. (Nes) 1 Northeast Iowa Podiatry 1 Northeast Resins & Silicones, LLC 1

Northeast Orthotics and Prothetics, Inc.

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 “Northeast”