FDA device listing
Sol-Care Safety Needle
FDA device listing 1445403250 · ZHEJIANG KINDLY MEDICAL DEVICES CO., LTD
Key facts
| Proprietary names | Sol-Care Safety Needle |
|---|---|
| Owner/operator | ZHEJIANG KINDLY MEDICAL DEVICES CO., LTD |
| Owner/operator number | 9036461 |
| Product codes | FMI |
| Device names | FMI - Needle, Hypodermic, Single Lumen |
| Device class | Class II |
| Classification regulations (21 CFR) | 880.5570 |
| Review panels | General Hospital |
| Registered establishments | ZHEJIANG KINDLY MEDICAL DEVICES CO., LTD |
| Establishment registrations | 9615588 |
| FEI numbers | 3003560965 |
| Establishment operations | Contract Manufacturer, Contract Sterilizer |
| 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