# Norlase Aps

> Medical device manufacturer record on deviCERTS, compiled from public registries. Norlase Aps is a medical device manufacturer, with 9 devices listed in FDA GUDID and FDA 510(k) (FDA Class II) as of 14 Nov 2026.

- Canonical page: <https://devicerts.com/manufacturers/norlase-aps>
- Country: Denmark (FDA applicant, unverified)
- Role: Manufacturer
- Registrations: FDA
- FDA FEI: 3015658550
- DUNS: 305483903

## Figures

- Devices: 9
- 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 GUDID 6, FDA 510(k) 3
- Device classes: FDA Class II 9

## Devices

The first 9 of 9, in the order of the canonical page, which lists them all.

- [Norlase ECHO photocoagulator N007-9200](https://devicerts.com/devices/norlase-echo-photocoagulator-n007-9200) · Class II · GUDID · status: Listed
- [Norlase Leaf photocoagulator N005-9010-03](https://devicerts.com/devices/norlase-leaf-photocoagulator-n005-9010-03) · Class II · GUDID · status: Active
- [Norlase ECHO photocoagulator N007-9200-Z](https://devicerts.com/devices/norlase-echo-photocoagulator-n007-9200-z) · Class II · GUDID · status: Listed
- [Norlase LYNX photocoagulator N008-9200](https://devicerts.com/devices/norlase-lynx-photocoagulator-n008-9200) · Class II · GUDID · status: Listed
- [Norlase LION photocoagulator N006-9200](https://devicerts.com/devices/norlase-lion-photocoagulator-n006-9200) · Class II · GUDID · status: Listed
- [Norlase LEAF photocoagulator N005-9010-Z](https://devicerts.com/devices/norlase-leaf-photocoagulator-n005-9010-z) · Class II · GUDID · status: Active
- [LYNX Photocoagulator](https://devicerts.com/devices/lynx-photocoagulator-hqf) · ref K242397 · Class II · 510(k) · status: Active · decision 2024-10-25
- [LION Photocoagulator](https://devicerts.com/devices/lion-photocoagulator-hqf) · ref K201623 · Class II · 510(k) · status: Active · decision 2020-08-11
- [Leaf Photocoagulator](https://devicerts.com/devices/leaf-photocoagulator-hqf) · ref K190083 · Class II · 510(k) · status: Active · decision 2019-05-03

## Source and citation

- Cite as: Norlase Aps. deviCERTS medical device catalogue. https://devicerts.com/manufacturers/norlase-aps (data as of 2026-11-14).
- Data sources: [FDA GUDID](https://accessgudid.nlm.nih.gov/), [FDA 510(k)](https://open.fda.gov/apis/device/510k/), [FDA registration and listing](https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfrl/rl.cfm)
- FDA recall data as of: 2026-11-01
- Data as of: 2026-11-14
- JSON: <https://devicerts.com/manufacturers/norlase-aps.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/norlase-aps
- 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.