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

FDA 510(k)

LightStim for Wrinkles (1984); LightStim for Acne (2038)

K-Number: K261482 · 2026-07-31

Decision Date2026-07-31
Product CodeOHS
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LightStim for Wrinkles (1984); LightStim for Acne (2038) is the device name listed in this FDA 510(k) record. The listed applicant is Led Intellectual Properties, LLC. It received FDA 510(k) clearance on 2026-07-31 under 510(k) number K261482. 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 LightStim for Wrinkles (1984); LightStim for Acne (2038)?

LightStim for Wrinkles (1984); LightStim for Acne (2038) is a medical device that received FDA 510(k) clearance on 2026-07-31. The listed applicant is Led Intellectual Properties, LLC. The 510(k) number is K261482.

When did LightStim for Wrinkles (1984); LightStim for Acne (2038) receive FDA 510(k) clearance?

LightStim for Wrinkles (1984); LightStim for Acne (2038) received FDA 510(k) clearance on 2026-07-31, under 510(k) number K261482.

Who is the listed applicant for LightStim for Wrinkles (1984); LightStim for Acne (2038)?

The FDA 510(k) record lists Led Intellectual Properties, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LightStim for Wrinkles (1984); LightStim for Acne (2038)?

The FDA product code for LightStim for Wrinkles (1984); LightStim for Acne (2038) is OHS.

Other records listing Led Intellectual Properties, LLC as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: OHS)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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.