FDA device listing
Tub. Elastic Ban 10 m 100 mm,Tub. Elastic Ban 10 m 45 mm,Tub. Elastic Ban 10 m 63 mm,Tub. Elastic Ban 10 m 75 mm,Tub…
FDA device listing 1770487377 · Tynor Orthotics (P) Ltd.
Key facts
| Proprietary names | Tub. Elastic Ban 10 m 100 mm,Tub. Elastic Ban 10 m 45 mm,Tub. Elastic Ban 10 m 63 mm,Tub. Elastic Ban 10 m 75 mm,Tub. Elastic Ban 10 m 88 mm,Tub. Elastic Ban 1 m 100 mm,Tub. Elastic Ban 1 m 45 mm,Tub. Elastic Ban 1 m 63 mm,Tub. Elastic Ban 1 m 75 mm,Tub. Elastic Ban 1 m 88 mm |
|---|---|
| Owner/operator | Tynor Orthotics (P) Ltd. |
| Owner/operator number | 9070795 |
| Product codes | ILG |
| Device names | ILG - Stocking, Elastic |
| Device class | Class I |
| Classification regulations (21 CFR) | 890.3475 |
| Review panels | Physical Medicine |
| Registered establishments | TYNOR ORTHOTICS (P) LTD. |
| Establishment registrations | 3005037196 |
| FEI numbers | 3005037196 |
| 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