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Data / Medical devices / United Kingdom / The Light Salon Boost Limited

The Light Salon Boost Limited: FDA-registered device maker in Rye East Sussex, United Kingdom, 2 510(k) clearances

The Light Salon Boost Limited is registered with the FDA (registration 3015783545) in Rye East Sussex, United Kingdom. It lists 3 device types. The FDA files 2 510(k) clearances under its listings, the newest dated December 20, 2022. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3015783545
Address
Herons New England Lane, Rye East Sussex, United Kingdom, TN31 7NT
Owner or operator
The Light Salon Boost Limited (10061893)
Roles
Repackager or relabeler
First device listed
November 29, 2019
Registered through
2026
Brand names listed
Boost The Light Salon Advanced LED Face Mask, Light Salon Boost, The Light Salon Boost LED Bib

Devices it lists

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
December 20, 2022K221775LED Light Therapy Mask (model: MK-78, MK-04, MK66-H, MK66R-B, EL00003)OHSSubstantially EquivalentLight Tree Ventures Europe B.V.accessdata.fda.gov
September 12, 2019K191629faceLITEOHSSubstantially EquivalentIsmart Marketing Svcs, Ltd.accessdata.fda.gov

Compare with other makers

Updated December 20, 2022. 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.