FDA applicant

Atlantis Luminescent Products, LLC

Houston, TX1 decision2005–20053 recalls

FDA records 1 decision for Atlantis Luminescent Products, LLC (Houston, TX) in 2005: 1 510(k) clearance. All are in product code ILY (Lamp, Infrared, Therapeutic Heating). Its devices cite 2 predicates, 0 of them its own earlier devices. 3 recalls are linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, physical medicine panel, where it files most

How often FDA has decided Atlantis Luminescent Products, LLC’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Atlantis Luminescent Products, LLC since 2007.

Recalls per year

3in 2012

2007high 3 (2012) · low 0 (2007)2026

Class I Class II/III not classified

FIG. 1 — Atlantis Luminescent Products, LLC by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Atlantis Luminescent Products, 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 “Atlantis”

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

Atlantis Components, Inc. 18 Atlantis Diagnostics Intl., Inc. 3 Atlantis Scientific Corp. 1

Atlantis Luminescent Products, LLC

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

What has been recalled?

Other applicant names beginning “Atlantis”