FDA device listing
Fassier-Duval Telescopic IM System
FDA device listing 1192622905 · Nordion Canada Inc.
Key facts
| Proprietary names | Fassier-Duval Telescopic IM System |
|---|---|
| Owner/operator | Nordion Canada Inc. |
| Owner/operator number | 8022247 |
| Product codes | HSB |
| Device names | HSB - Rod, Fixation, Intramedullary And Accessories |
| Device class | Class II |
| Classification regulations (21 CFR) | 888.3020 |
| Review panels | Orthopedic |
| Registered establishments | Gamma Centre of Excellence |
| Establishment registrations | 3010131578 |
| FEI numbers | 3010131578 |
| Establishment operations | 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