510(k) Report

FDA applicant

Laser Health Technologies, LLC

Chevy Chase, MD2 decisions2009–20100 recalls

FDA records 2 decisions for Laser Health Technologies, LLC (Chevy Chase, MD) from 2009 to 2010: 2 510(k) clearances. Most are in product codes GZJ (Stimulator, Nerve, Transcutaneous, For Pain…) and NUH (Stimulator, Nerve, Transcutaneous…). Its devices cite 7 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, neurology panel, where it files most

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

FDA decisions per year

1in 2010

2009: 12010: 1
2009high 1 (2009) · low 0 (2011)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2009.

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

Planning a device like Laser Health Technologies, LLC’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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Other applicant names beginning “Laser”

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