Lokki
Country not established
- Devices
- 2
What Lokki makes
Lokki manufactures the Lokki DT, a diagnostic tool for assessing nerve conduction, and the FLIPO Xenon Curing Light, a device used for polymerizing dental composites with xenon arc technology.
The company’s portfolio is regulated under FDA 510(k) clearance as Class II medical devices. These products are listed in the FDA’s 510(k) database and are based in the United States.
Catalogue
Lokki Dt Ref K952682
Regimes: 510(k) Registry: 510(k)Flipo Xenon Curing Light Ref K994028
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Lokki have in the registry?
The registry currently lists 2 devices for Lokki. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lokki's devices?
Among its 2 most recently registered devices, Lokki has devices listed in FDA 510(k) (2 devices).
What risk classes do Lokki's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Lokki's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Lokki in the registry?
The most recently registered devices listed for Lokki include LOKKI DT and FLIPO XENON CURING LIGHT.