# Lensar

> Medical device manufacturer record on deviCERTS, compiled from public registries. 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.

- Canonical page: <https://devicerts.com/manufacturers/lensar>
- Also registered as: LENSAR, Inc
- Country: United States (from SRN)
- EUDAMED actor status: active
- Role: Manufacturer
- Registrations: EUDAMED
- EUDAMED SRN: US-MF-000008522

## Figures

- Devices: 17
- FDA recalls (matched to the firm by name): 0

## Registry facts

*Every device of the manufacturer. A device listed in two registries counts in both.*

- Registries: FDA 510(k) 10, FDA GUDID 7, EUDAMED 5
- Device classes: FDA Class II 12, EU Class IIb 5
- EMDN [Z12 Instruments for functional explorations and therapeutic interventions](https://devicerts.com/categories/emdn/Z12): 5 devices

## Sites and related companies

- Authorised representative: [Emergo Europe B.V.](https://devicerts.com/representatives/emergo-europe-bv-nl-ar-000000116) (Netherlands)

## Devices

The first 17 of 17, in the order of the canonical page, which lists them all.

- [LENSAR LLS-fs 3D 70-00013-001](https://devicerts.com/devices/lensar-lls-fs-3d-70-00013-001) · Class II · GUDID · status: Active
- [LENSAR LLS-fs 3D 70-00005-001](https://devicerts.com/devices/lensar-lls-fs-3d-70-00005-001) · Class II · GUDID · status: Active
- [Patient Interface Device](https://devicerts.com/devices/patient-interface-device-70-00044-001) · ref 70-00044-001 · Class IIb · EUDAMED, GUDID · status: Active
- [Patient Interface Device](https://devicerts.com/devices/patient-interface-device-70-00046-001) · ref 70-00046-001 · Class IIb · EUDAMED, GUDID · status: Active
- [Patient Interface Device](https://devicerts.com/devices/patient-interface-device-70-00036-001) · ref 70-00036-001 · Class IIb · EUDAMED, GUDID · status: Active
- [Lensar Laser System - Fs 3D For Corneal Incisions](https://devicerts.com/devices/lensar-laser-system-fs-3d-for-corneal-incisions-hqc) · ref K122829 · Class II · 510(k) · status: Active · decision 2012-12-03
- [LENSAR Laser System - fs 3D (LLS-fs 3D)](https://devicerts.com/devices/lensar-laser-system-fs-3d-lls-fs-3d-ooe-k152453) · ref K152453 · Class II · 510(k) · status: Active · decision 2015-10-15
- [LENSAR Laser System - fs 3D (LLS-fs 3D)](https://devicerts.com/devices/lensar-laser-system-fs-3d-lls-fs-3d-ooe-k181430) · ref K181430 · Class II · 510(k) · status: Active · decision 2018-08-09
- [LENSAR Laser System - fs 3D (LLS-fs 3D)](https://devicerts.com/devices/lensar-laser-system-fs-3d-lls-fs-3d-ooe-k173346) · ref K173346 · Class II · 510(k) · status: Active · decision 2018-03-02
- [Lensar Laser System](https://devicerts.com/devices/lensar-laser-system-ooe) · ref K090633 · Class II · 510(k) · status: Active · decision 2010-05-13
- [LENSAR Laser System - fs 3D](https://devicerts.com/devices/lensar-laser-system-fs-3d-ooe) · ref K143010 · Class II · 510(k) · status: Active · decision 2015-03-20
- [LENSAR Laser System – fs 3D (LLS-fs 3D)](https://devicerts.com/devices/lensar-laser-system-fs-3d-lls-fs-3d-ooe-k171337) · ref K171337 · Class II · 510(k) · status: Active · decision 2017-08-10
- [Lensar Laser System For Anterior Capsulotomy](https://devicerts.com/devices/lensar-laser-system-for-anterior-capsulotomy-ooe) · ref K102727 · Class II · 510(k) · status: Active · decision 2011-03-16
- [LENSAR Laser System - fs 3D (LLS-fs 3D)](https://devicerts.com/devices/lensar-laser-system-fs-3d-lls-fs-3d-ooe-k182795) · ref K182795 · Class II · 510(k) · status: Active · decision 2018-12-21
- [LENSAR Laser System - fs 3D (LLS-fs 3D)](https://devicerts.com/devices/lensar-laser-system-fs-3d-lls-fs-3d-ooe) · ref K170576 · Class II · 510(k) · status: Active · decision 2017-05-05
- [ALLY Drapes](https://devicerts.com/devices/ally-drapes-70-00055-001) · ref 70-00055-001 · Class IIb · EUDAMED, GUDID · status: Active
- [ALLY Adaptive Cataract Treatment System](https://devicerts.com/devices/ally-adaptive-cataract-treatment-system-70-00050-001) · ref 70-00050-001 · Class IIb · EUDAMED, GUDID · status: Active

## Source and citation

- Cite as: Lensar. deviCERTS medical device catalogue. https://devicerts.com/manufacturers/lensar (data as of 2026-11-14).
- Data sources: [EUDAMED](https://ec.europa.eu/tools/eudamed), [FDA 510(k)](https://open.fda.gov/apis/device/510k/), [FDA GUDID](https://accessgudid.nlm.nih.gov/)
- EUDAMED record synced: 2026-11-07
- FDA recall data as of: 2026-11-01
- Data as of: 2026-11-14
- JSON: <https://devicerts.com/manufacturers/lensar.json>
- Licence: [CC BY 4.0](https://creativecommons.org/licenses/by/4.0/). The deviCERTS layout and text are licensed under CC BY 4.0. Registry data remain under their source terms: U.S. FDA data (openFDA, AccessGUDID) are U.S. public domain; EUDAMED data are subject to the European Commission reuse terms.
- Attribution: DevicErts, https://devicerts.com/manufacturers/lensar
- Compiled by deviCERTS (devicerts.com) from public medical device registries (EUDAMED, European Commission; U.S. FDA via openFDA; AccessGUDID, U.S. National Library of Medicine). deviCERTS is not an official register and gives no regulatory advice: the record in the registry itself prevails.