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FDA 510(k)

Light Therapy System (M500, L6)

K-Number: K251042 · 2025-06-06

ApplicantGuangzhou Ahead Intelligent Technology Co., Ltd.
Decision Date2025-06-06
Product CodeOHS
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Light Therapy System (M500, L6) is a medical device manufactured by Guangzhou Ahead Intelligent Technology Co., Ltd.. It received FDA 510(k) clearance on 2025-06-06 under approval number K251042. The device is classified under product code OHS. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Light Therapy System (M500, L6)?

Light Therapy System (M500, L6) is a medical device that received FDA 510(k) clearance on 2025-06-06. It is manufactured by Guangzhou Ahead Intelligent Technology Co., Ltd.. The 510(k) number is K251042.

When was Light Therapy System (M500, L6) approved by the FDA?

Light Therapy System (M500, L6) received FDA 510(k) clearance on 2025-06-06, under approval number K251042.

What company makes Light Therapy System (M500, L6)?

Light Therapy System (M500, L6) is manufactured by Guangzhou Ahead Intelligent Technology Co., Ltd..

What is the FDA product code for Light Therapy System (M500, L6)?

The FDA product code for Light Therapy System (M500, L6) is OHS.

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Related PubMed Literature

PMID: 41966529 Comparison of the AccuPower HIV-1 Quant Kit and Aptima HIV-1 Quant Dx Assay for quantification of HIV-1 plasma viral load. Diagnostic microbiology and infectious disease (2026) PMID: 40942702 Digital Cardiovascular Twins, AI Agents, and Sensor Data: A Narrative Review from System Architecture to Proactive Heart Health. Sensors (Basel, Switzerland) (2025) PMID: 40624966 Peptide-Enhanced Bioactive Hydrogel Combined with Photodynamic-Phage Synergistic Antibacterial Therapy System Accelerates Infected Wound Healing. Advanced healthcare materials (2025) PMID: 40417352 Regulatory aspects of optogenetic research and therapy for retinitis pigmentosa under EU law. Frontiers in medical technology (2025)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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