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Data / Medical devices / Over-The-Counter Powered Light Based Laser For Acne / United States

FDA-registered makers of Over-The-Counter Powered Light Based Laser For Acne in the United States: 11 establishments

11 establishments in the United States are registered with the FDA to make Over-The-Counter Powered Light Based Laser For Acne (product code OLP). 6 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.

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Device
Over-The-Counter Powered Light Based Laser For Acne
Product code
OLP
Country
United States

Makers of Over-The-Counter Powered Light Based Laser For Acne in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Led Technologies, Inc.Largo, FL, United StatesManufacturer3December 21, 2021000api.fda.gov
Heat In A Click LLCDania, FL, United StatesSpecification developer2July 7, 2022000api.fda.gov
Erchonia CorporationFountain Inn, SC, United StatesComplaint file establishment, Manufacturer, Remanufacturer1September 12, 2025000api.fda.gov
Led Intellectual Properties LLCIrvine, CA, United StatesComplaint file establishment, Manufacturer1January 29, 2015000api.fda.gov
Luminance Medical Ventures IncorporatedThe Colony, TX, United StatesComplaint file establishment, Specification developer1June 9, 2022000api.fda.gov
Michael Todd Beauty, LPPort St Lucie, FL, United StatesSpecification developer1February 15, 2016000api.fda.gov
Alc Enterprises IncBrooklyn, NY, United StatesSpecification developer0000api.fda.gov
Amazing Impulse, LLCLake Mary, FL, United StatesContract manufacturer, Contract sterilizer0000api.fda.gov
Biophotas, Inc.Tustin, CA, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Sharkninja Operating LLCNeedham, MA, United StatesManufacturer, Specification developer0000api.fda.gov
Therabody, Inc.Los Angeles, CA, United StatesComplaint file establishment, Specification developer0000api.fda.gov

Updated November 2, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.