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Data / Medical devices / Light Based Over The Counter Wrinkle Reduction / United States

FDA-registered makers of Light Based Over The Counter Wrinkle Reduction in the United States: 14 establishments

14 establishments in the United States are registered with the FDA to make Light Based Over The Counter Wrinkle Reduction (product code OHS). 9 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

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Device
Light Based Over The Counter Wrinkle Reduction
Product code
OHS
Country
United States

Makers of Light Based Over The Counter Wrinkle Reduction in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Led Technologies, Inc.Largo, FL, United StatesManufacturer7December 21, 2022000api.fda.gov
Led Intellectual Properties LLCIrvine, CA, United StatesComplaint file establishment, Manufacturer5July 31, 2026000api.fda.gov
Carol Cole Company dba NuFACEVista, CA, United StatesComplaint file establishment, Manufacturer, Repackager or relabeler, Specification developer2April 2, 2022000api.fda.gov
Merchsource LLCIrvine, CA, United StatesSpecification developer2October 16, 2025000api.fda.gov
NIRA Innovations IncDerry, NH, United StatesManufacturer2February 8, 2023000api.fda.gov
Therabody, Inc.Los Angeles, CA, United StatesComplaint file establishment, Specification developer2June 9, 2023000api.fda.gov
Biophotas, Inc.Tustin, CA, United StatesComplaint file establishment, Manufacturer1September 1, 2017000api.fda.gov
Carewear Corp.Reno, NV, United StatesSpecification developer1November 19, 2020000api.fda.gov
Sharkninja Operating LLCNeedham, MA, United StatesManufacturer, Specification developer1November 27, 2024000api.fda.gov
Alc Enterprises IncBrooklyn, NY, United StatesSpecification developer0000api.fda.gov
Amazing Impulse, LLCLake Mary, FL, United StatesContract manufacturer, Contract sterilizer0000api.fda.gov
Avazzia, Inc.Dallas, TX, United StatesManufacturer0000api.fda.gov
Heat In A Click LLCDania, FL, United StatesSpecification developer0000api.fda.gov
Xtreem PulseNew York, NY, United StatesManufacturer0000api.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.