FDA device listing
AMSCO LD202 In-Ceiling Lighting System (MG-CFE),AMSCO LD202 Wall Controller (MG-CFE),Hexalux Examination Light…
FDA device listing 1421026981 · STERIS Corporation
Key facts
| Proprietary names | AMSCO LD202 In-Ceiling Lighting System (MG-CFE),AMSCO LD202 Wall Controller (MG-CFE),Hexalux Examination Light (MG-MF),Hexalux Mobile Stand (MG-MF),LED202 In-Ceiling Dual Lighting System (MG-MF),LED202 In-Ceiling Single Lighting System (MG-MF) |
|---|---|
| Owner/operator | STERIS Corporation |
| Owner/operator number | 10078069 |
| 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 | STERIS CORPORATION |
| Establishment registrations | 1043572 |
| FEI numbers | 1043572 |
| Establishment operations | Complaint File Establishment, 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