FDA device listing
3-Head LED Examination Lamp; 5-Head LED Examination Lamp; EXAMINATION LAMP; EndoNest Examination Lamp,EndoNest…
FDA device listing 2051174257 · ENDONEST MEDICAL SYSTEMS LLP
Key facts
| Proprietary names | 3-Head LED Examination Lamp; 5-Head LED Examination Lamp; EXAMINATION LAMP; EndoNest Examination Lamp,EndoNest Examination Light, floor Light , Cealing Lights, Single Dom, Double Dome, Mount Light,EndoNest Exam Lights (Light IV, 300, 600, 900) and Accessories; EndoNest Examination Light and accessories,Led Light Source Portable ,EndoNest Led Portable Light,White Light, Floor Light… |
|---|---|
| Owner/operator | ENDONEST MEDICAL SYSTEMS LLP |
| Owner/operator number | 10090090 |
| Product codes | KZF |
| Device names | KZF - Device, Medical Examination, Ac Powered |
| Device class | Class I |
| Classification regulations (21 CFR) | 880.6320 |
| Review panels | General Hospital |
| 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