Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Aglaia LED Beauty Device (BP-D2309)

K-Number: K250413 · 2025-03-18

Decision Date2025-03-18
Product CodeOHS
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Aglaia LED Beauty Device (BP-D2309) is a medical device manufactured by Shenzhen Perfect Idea Technology Limited. It received FDA 510(k) clearance on 2025-03-18 under approval number K250413. 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 Aglaia LED Beauty Device (BP-D2309)?

Aglaia LED Beauty Device (BP-D2309) is a medical device that received FDA 510(k) clearance on 2025-03-18. It is manufactured by Shenzhen Perfect Idea Technology Limited. The 510(k) number is K250413.

When was Aglaia LED Beauty Device (BP-D2309) approved by the FDA?

Aglaia LED Beauty Device (BP-D2309) received FDA 510(k) clearance on 2025-03-18, under approval number K250413.

What company makes Aglaia LED Beauty Device (BP-D2309)?

Aglaia LED Beauty Device (BP-D2309) is manufactured by Shenzhen Perfect Idea Technology Limited.

What is the FDA product code for Aglaia LED Beauty Device (BP-D2309)?

The FDA product code for Aglaia LED Beauty Device (BP-D2309) is OHS.

Related Devices (Code: OHS)

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.