Surgical Laser Incorporated
Country not established
- Devices
- 1
What Surgical Laser Incorporated makes
Surgical Laser Incorporated manufactures laser fibers and endoprobes for medical applications, including bare fibers (DENT, HO, HCS) and a lateral firing fiber designed for precision surgical procedures. These devices are intended for use in laser-based treatments, such as dermatology, ophthalmology, and minimally invasive surgeries.
The company’s products are classified as Class II medical devices under FDA regulations and are listed via the 510(k) pathway. These devices are registered in the FDA’s 510(k) database, adhering to U.S. regulatory standards for laser-based medical instruments.
Catalogue
SLI Endoprobe, SLI DENT Bare Fiber, SLI HO Bare Fiber, SLI HCS Bare Fiber, SLI Lateral Firing Fiber Ref K151855
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Surgical Laser Incorporated have in the registry?
The registry currently lists 1 device for Surgical Laser Incorporated. Devices recorded under merged duplicate company entries are counted once.
Which registries list Surgical Laser Incorporated's devices?
Among its 1 most recently registered device, Surgical Laser Incorporated has devices listed in FDA 510(k) (1 device).
What risk classes do Surgical Laser Incorporated's devices fall under?
Among its 1 most recently registered device, the classes recorded for Surgical Laser Incorporated's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Surgical Laser Incorporated in the registry?
The most recently registered devices listed for Surgical Laser Incorporated include SLI Endoprobe, SLI DENT Bare Fiber, SLI HO Bare Fiber, SLI HCS Bare Fiber, SLI Lateral Firing Fiber.