510(k) Report

FDA applicant

Ag Digital Technology Corp.

Flagstaff, AZ4 decisions2009–20130 recalls

FDA records 4 decisions for Ag Digital Technology Corp. (Flagstaff, AZ) from 2009 to 2013: 4 510(k) clearances. Most are in product codes MQV (Filler, Bone Void, Calcium Compound) and LHQ (System, Telethermographic (Adjunctive Use)). Its devices cite 5 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, orthopedic panel, where it files most

How often FDA has decided Ag Digital Technology Corp.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2013

2009: 12010: 12011: 12013: 1
2009high 1 (2009) · low 0 (2012)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2009.

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

Planning a device like Ag Digital Technology Corp.’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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