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

FDA-registered makers of Light Based Over The Counter Wrinkle Reduction in the United Kingdom: 6 establishments

6 establishments in the United Kingdom are registered with the FDA to make Light Based Over The Counter Wrinkle Reduction (product code OHS). 6 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.

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

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

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
The Beauty Tech Group LtdMacclesfield Cheshire East, United KingdomExporter to the US, Specification developer7June 3, 2026000api.fda.gov
I-SMART Development LTD.Sutton Coldfield Birmingham, United KingdomManufacturer, Specification developer4July 24, 2026000api.fda.gov
Lyma Life Ltd.London London, City of, United KingdomManufacturer2February 21, 2025000api.fda.gov
Lustre Skin LtdLivingston Scotland, United KingdomComplaint file establishment, Exporter to the US, Repackager or relabeler, Specification developer2March 15, 2023000api.fda.gov
Aesthetic Technology LtdWarrington Cheshire East, United KingdomManufacturer1November 18, 2021000api.fda.gov
Opatra LtdLondon London, City of, United KingdomManufacturer1December 20, 2022000api.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.