FDA applicant

Lexicor Medical Technology, Inc.

Boulder, CO4 decisions1991–20130 recalls

FDA records 4 decisions for Lexicor Medical Technology, Inc. (Boulder, CO) from 1991 to 2013: 3 510(k) clearances and 1 De Novo grant. Most are in product codes HCC (Device, Biofeedback) and GWQ (Full-Montage Standard Electroencephalograph). Its devices cite 1 predicate, 0 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Lexicor Medical Technology, LLC”.

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 Lexicor Medical Technology, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2013

2007high 1 (2013) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Lexicor Medical Technology, Inc.’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

Other applicant names beginning “Lexicor”

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

Lexicor 1

Lexicor Medical Technology, 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 “Lexicor”