FDA device listing
Anti Embolism stockings; Knee High; light type pressure, Level 1; medium type pressure, Level 2; Thigh High;,light type…
FDA device listing 1056908266 · Jinhua Beili Knitting Co.,Ltd.
Key facts
| Proprietary names | Anti Embolism stockings; Knee High; light type pressure, Level 1; medium type pressure, Level 2; Thigh High;,light type pressure, Level 1; medium type pressure, Level 2 |
|---|---|
| Owner/operator | Jinhua Beili Knitting Co.,Ltd. |
| Owner/operator number | 10091872 |
| Product codes | IOD |
| Device names | IOD - Components, Exercise |
| Device class | Class I |
| Classification regulations (21 CFR) | 890.5350 |
| Review panels | Physical Medicine |
| Registered establishments | JINHUA BEILI KNITTING CO.,LTD. |
| Establishment registrations | 3013440000 |
| FEI numbers | 3013440000 |
| 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