FDA device listing
Abduction Pillow,Bobath Sling,B-Sling,Hemi Sling,Kenny Howard,L-Sling,O-Sling,Shoulder O-Sling,Ultra-Sling
FDA device listing 2043866597 · ORTEC Co., LTD.
Key facts
| Proprietary names | Abduction Pillow,Bobath Sling,B-Sling,Hemi Sling,Kenny Howard,L-Sling,O-Sling,Shoulder O-Sling,Ultra-Sling |
|---|---|
| Owner/operator | ORTEC Co., LTD. |
| Owner/operator number | 10036960 |
| Product codes | ILI |
| Device names | ILI - Sling, Arm |
| Device class | Class I |
| Classification regulations (21 CFR) | 890.3640 |
| Review panels | Physical Medicine |
| Registered establishments | ORTEC Co., LTD. |
| Establishment registrations | 3009119999 |
| FEI numbers | 3009119999 |
| 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