FDA applicant

Nuvectra Corporation

Blaine1 decision2015–20155 recalls

FDA records 1 decision for Nuvectra Corporation (Blaine) in 2015: 1 original PMA approval. All are in product code LGW (Stimulator, Spinal-Cord, Totally Implanted For…). 5 recalls are 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 Nuvectra Corporation’s devices, and how often a recall has named them.

FDA decisions per year

1in 2015

2015high 1 (2015) · low 0 (2016)2026

2026 so far, outlined.

Recalls per year

5in 2016

2015high 5 (2016) · low 0 (2015)2026

Class I Class II/III not classified

FIG. 1 — Nuvectra Corporation by year, 2015–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Nuvectra Corporation

Which product codes does it file in?

What has FDA decided for it lately?

What has been recalled?