Fiberlase U.S.A.
Country not established
- Devices
- 1
What Fiberlase U.S.A. makes
Fiberlase U.S.A. manufactures the FIBERLAS 100 Medical System, a device designed for medical laser applications, including tissue ablation and coagulation procedures.
The FIBERLAS 100 Medical System is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Fiberlas 100 Medical System Ref K833499
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Fiberlase U.S.A. have in the registry?
The registry currently lists 1 device for Fiberlase U.S.A.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Fiberlase U.S.A.'s devices?
Among its 1 most recently registered device, Fiberlase U.S.A. has devices listed in FDA 510(k) (1 device).
What risk classes do Fiberlase U.S.A.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Fiberlase U.S.A.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Fiberlase U.S.A. in the registry?
The most recently registered devices listed for Fiberlase U.S.A. include FIBERLAS 100 MEDICAL SYSTEM.