510(k) Report

FDA applicant

Numia Medical Technology, LLC

Lyndonville, VT1 decision2009–20090 recalls

FDA records 1 decision for Numia Medical Technology, LLC (Lyndonville, VT) in 2009: 1 510(k) clearance. All are in product code FRN (Pump, Infusion). 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, general hospital panel, where it files most

How often FDA has decided Numia Medical Technology, LLC’s devices, and how often a recall has named them.

FDA decisions per year

1in 2009

2009: 1
2009high 1 (2009) · low 0 (2010)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2009.

FIG. 1 — Numia Medical Technology, LLC by year, 2009–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Numia Medical Technology, LLC’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?

  • FRNPump, Infusion1decision

What has FDA decided for it lately?

  • K091386Microfuse Dual Rate InfuserNumia Medical Technology, LLC · 2009

The one decision as Numia Medical Technology, LLC →