FDA device listing
EndoNest Diode LAser (Sunbeam-15w/980nm),(Sunbeam-10w/980nm+10w/1470nm), (Sunbeam-Tripal wavelenght),EndoNest Skin Laser…
FDA device listing 1705892414 · ENDONEST MEDICAL SYSTEMS LLP
Key facts
| Proprietary names | EndoNest Diode LAser (Sunbeam-15w/980nm),(Sunbeam-10w/980nm+10w/1470nm), (Sunbeam-Tripal wavelenght),EndoNest Skin Laser (Subnbeam-SLDL), Diode Laser (sunbeam - 1620D), (Sunbeam-16201),(Sunbeam-16202),(Sunbeam-16302),EndoNest Therapy Laser,(Sunbeam-12w/980nm),(Sunbeam-12w/980nm+10w/1470nm),,EndoNest Thullium Laser, Thullium Laser 70W, Thullium Laser 40W , sunbeam 10W EndoNest ENT Laser,(Sunbeam… |
|---|---|
| Owner/operator | ENDONEST MEDICAL SYSTEMS LLP |
| Owner/operator number | 10090090 |
| Product codes | NXF |
| Device names | NXF - Gas, Laser Generating |
| Device class | Class I |
| Classification regulations (21 CFR) | 878.4810 |
| Review panels | General & Plastic Surgery |
| Registered establishments | ENDONEST MEDICAL SYSTEMS LLP |
| Establishment registrations | 3030516433 |
| FEI numbers | 3030516433 |
| Establishment operations | Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None listed Premarket submission listed
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device listings
Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database