Biolitec Sia
Country not established
- Devices
- 1
What Biolitec Sia makes
Biolitec Sia manufactures an endovascular laser venous system kit, including a radial emitting fiber designed for vascular procedures. The kit is intended for use in treating venous conditions through controlled laser energy delivery.
The company’s products fall under FDA Class II regulation and are listed via 510(k) clearance. Biolitec Sia is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Biolitec Sia have in the registry?
The registry currently lists 1 device for Biolitec Sia. Devices recorded under merged duplicate company entries are counted once.
Which registries list Biolitec Sia's devices?
Among its 1 most recently registered device, Biolitec Sia has devices listed in FDA 510(k) (1 device).
What risk classes do Biolitec Sia's devices fall under?
Among its 1 most recently registered device, the classes recorded for Biolitec Sia's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Biolitec Sia in the registry?
The most recently registered devices listed for Biolitec Sia include ENDOVASCULAR LASER VENOUS SYSTEM KIT WITH 2 RING RADIAL EMITTING FIBER.