FDA device listing
examination light(Model:KL01L Series KL-201 Series, KL-301 Series, KL-303 Series, KL-307 Series,KL-312 Series)
FDA device listing 1210566020 · Jiangsu Keling Medical Appliances Co.,Ltd.
Key facts
| Proprietary names | examination light(Model:KL01L Series KL-201 Series, KL-301 Series, KL-303 Series, KL-307 Series,KL-312 Series) |
|---|---|
| Owner/operator | Jiangsu Keling Medical Appliances Co.,Ltd. |
| Owner/operator number | 10050477 |
| 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 | JIANGSU KELING MEDICAL APPLIANCES CO.,LTD. |
| Establishment registrations | 3010373530 |
| FEI numbers | 3010373530 |
| 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