Lasertek Oy
Country not established
- Devices
- 3
What Lasertek Oy makes
Lasertek OY manufactures argon and laser coagulators, including the Model 40 AARGON, Model 41AK, and Model 150K. These devices are designed for tissue coagulation in medical procedures, using laser or argon beam technology to seal blood vessels and prevent bleeding.
The company’s coagulators are classified as Class II devices under FDA regulations and are listed via 510(k) clearance. The portfolio is regulated in the United States, where the manufacturer is based.
Catalogue
Coagulator, Model 40 Aargon Ref K782106
Regimes: 510(k) Registry: 510(k)Laser Coagulator, Model 41AK Ref K781965
Regimes: 510(k) Registry: 510(k)Model 150K Laser Coagulator Ref K832089
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Lasertek OY have in the registry?
The registry currently lists 3 devices for Lasertek OY. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lasertek OY's devices?
Among its 3 most recently registered devices, Lasertek OY has devices listed in FDA 510(k) (3 devices).
What risk classes do Lasertek OY's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Lasertek OY's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Lasertek OY in the registry?
The most recently registered devices listed for Lasertek OY include COAGULATOR, MODEL 40 AARGON, LASER COAGULATOR, MODEL 41AK and MODEL 150K LASER COAGULATOR.