Lmi Lightwave Medical Industries, Ltd.
CanadaFDA applicant, unverified
- Devices
- 1
What Lmi Lightwave Medical Industries, Ltd. makes
The company manufactures electrosurgical devices, including a hand-controlled pencil with a blade electrode and a controller for electrosurgical procedures.
These devices are classified as Class II under FDA regulations and are listed in the 510(k) premarket notification database. The company is based in the United States.
Catalogue
Lumitrol Controller, Lumitrol Hand-Controlled Electrosurgical Pencil With Blade Electrode Ref K953992
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Lmi Lightwave Medical Industries, Ltd. have in the registry?
The registry currently lists 1 device for Lmi Lightwave Medical Industries, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lmi Lightwave Medical Industries, Ltd.'s devices?
Among its 1 most recently registered device, Lmi Lightwave Medical Industries, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Lmi Lightwave Medical Industries, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Lmi Lightwave Medical Industries, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Lmi Lightwave Medical Industries, Ltd. in the registry?
The most recently registered devices listed for Lmi Lightwave Medical Industries, Ltd. include LUMITROL CONTROLLER, LUMITROL HAND-CONTROLLED ELECTROSURGICAL PENCIL WITH BLADE ELECTRODE.