Lensar
Active in EUDAMEDUnited Statesfrom SRN EUDAMED SRN US-MF-000008522
Lensar is a medical device manufacturer based in the United States, with 17 devices listed in FDA 510(k), FDA GUDID and EUDAMED (FDA Class II; EU Class IIb) as of 14 Nov 2026.
- Devices
- 17
- Registrations
- EUDAMED
Registry facts
- Registries
- FDA 510(k) 10
- FDA GUDID 7
- EUDAMED 5
- Device classes
- FDA Class II 12
- EU Class IIb 5
- Top EMDN categories
- Sites and related companies
- Emergo Europe B.V. authorised representative
- Identifiers
- EUDAMED SRN US-MF-000008522
At a glance
Market reach
- European Union
- EUDAMED actor
- Authorised rep.
- Emergo Europe B.V.NL
Catalogue
Search and filter all 17 devicesCompany details
- EUDAMED SRN
- US-MF-000008522
- EUDAMED status
- Active
- EUDAMED registered name
- LENSAR
- EUDAMED abbreviated name
- LENSAR
- Registered address
- 2800, Discovery Drive, 32826, Orlando, Fl., United States
- Website
- Lensar.com
- Phone
- +1 888 575 6412
- PRRC contact
- Keith Peck
Frequently asked questions
How many devices does LENSAR have in the registry?
The registry currently lists 17 devices for LENSAR. Devices recorded under merged duplicate company entries are counted once.
Which registries list LENSAR's devices?
Among its 17 most recently registered devices, LENSAR has devices listed in EUDAMED (5 devices), FDA 510(k) (10 devices) and FDA GUDID (7 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do LENSAR's devices fall under?
Among its 17 most recently registered devices, the classes recorded for LENSAR's devices are Class IIb and Class II. Each device page shows its own class and authorisation.
What are the newest devices from LENSAR in the registry?
The most recently registered devices listed for LENSAR include LENSAR LLS-fs 3D 70-00013-001, LENSAR LLS-fs 3D 70-00005-001, Patient Interface Device and LENSAR LASER SYSTEM - FS 3D FOR CORNEAL INCISIONS.