510(k) Report

FDA applicant

Applied Biophotonics, Ltd.

Central, CN1 decision2015–20150 recalls

FDA records 1 decision for Applied Biophotonics, Ltd. (Central, CN) in 2015: 1 510(k) clearance. All are in product code ILY (Lamp, Infrared, Therapeutic Heating). Its devices cite 4 predicates, 0 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, physical medicine panel, where it files most

How often FDA has decided Applied Biophotonics, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2015

2015: 1
2015high 1 (2015) · low 0 (2016)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2015.

FIG. 1 — Applied Biophotonics, Ltd. by year, 2015–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Applied Biophotonics, Ltd.’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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Which product codes does it file in?

  • ILYLamp, Infrared, Therapeutic Heating1decision

Whose devices does it build on?

Its devices cite 4 predicates; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K142256Applied BioPhotonics Phototherapy System ABPT1003Applied Biophotonics, Ltd. · 2015

The one decision as Applied Biophotonics, Ltd. →