Lyma Life, Ltd.
United KingdomFDA applicant, unverified FDA
- Devices
- 4
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA establishment
What Lyma Life, Ltd. makes
Lyma Life, Ltd. manufactures LYMA Laser and LYMA Laser PRO, which are medical lasers designed for specific dermatological and aesthetic applications, including skin rejuvenation and hair removal.
These devices are classified as Class II under US regulations and are listed via the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
- Registry: GUDID
- Registry: GUDID
LYMA Laser Ref K210823
Regimes: 510(k) Registry: 510(k)LYMA Laser PRO Ref K243330
Regimes: 510(k) Registry: 510(k)
FDA establishments
- Lyma Life Ltd. London London, City of · GB FEI 3015646995
Frequently asked questions
How many devices does Lyma Life, Ltd. have in the registry?
The registry currently lists 4 devices for Lyma Life, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lyma Life, Ltd.'s devices?
Among its 4 most recently registered devices, Lyma Life, Ltd. has devices listed in FDA 510(k) (2 devices) and FDA GUDID (2 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Lyma Life, Ltd.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Lyma Life, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Lyma Life, Ltd. in the registry?
The most recently registered devices listed for Lyma Life, Ltd. include LYMA Laser 1, LYMA Laser PRO 1, LYMA Laser and LYMA Laser PRO.
Which FDA establishments are linked to Lyma Life, Ltd.?
1 FDA establishment is linked to Lyma Life, Ltd. in the registry; they are listed on the company page.