510(k) Report

FDA applicant

Guidemia Technologies, LLC

Los Alamitos, CA2 decisions2012–20170 recalls

FDA records 2 decisions for Guidemia Technologies, LLC (Los Alamitos, CA) from 2012 to 2017: 2 510(k) clearances. Most are in product codes PNN (Orthodontic Software) and LLZ (System, Image Processing, Radiological). 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, dental panel, where it files most

How often FDA has decided Guidemia Technologies, LLC’s devices, and how often a recall has named them.

FDA decisions per year

1in 2017

2012: 12017: 1
2012high 1 (2012) · low 0 (2013)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2012.

FIG. 1 — Guidemia Technologies, LLC by year, 2012–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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