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Data / Medical devices / United Kingdom / Lyma Life Ltd.

Lyma Life Ltd.: FDA-registered device maker in London London, City of, United Kingdom, 2 510(k) clearances

Lyma Life Ltd. is registered with the FDA (registration 3015646995) in London London, City of, United Kingdom. It lists 3 device types. The FDA files 2 510(k) clearances under its listings, the newest dated February 21, 2025. Registered through 2027. FDA data exported November 2, 2026.

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FDA registration number
3015646995
Address
Old Marylebone Road Edison House, London London, City of, United Kingdom, NW1 5QT
Owner or operator
LYMA LIFE LTD. (10079472)
Roles
Manufacturer
First device listed
April 29, 2022
Registered through
2027
Brand names listed
LYMA Laser, LYMA Laser PRO

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
February 21, 2025K243330LYMA Laser PROOHSSubstantially EquivalentLyma Life , Ltd.accessdata.fda.gov
March 18, 2022K210823LYMA LaserOHSSubstantially EquivalentLyma Life , Ltd.accessdata.fda.gov

Compare with other makers

Updated February 21, 2025. 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.