FDA device listing
JUZO,Juzo Basic,Juzo Dynamic,Juzo Dynamic Silver,Juzo Expert,Juzo Expert Cotton,Juzo Expert Silver,Juzo Seamless,Juzo…
FDA device listing 1475648020 · JULIUS ZORN GMBH
Key facts
| Proprietary names | JUZO,Juzo Basic,Juzo Dynamic,Juzo Dynamic Silver,Juzo Expert,Juzo Expert Cotton,Juzo Expert Silver,Juzo Seamless,Juzo Sensation,Juzo Soft,Juzo Soft Seamless,Juzo Strong Silver |
|---|---|
| Owner/operator | JULIUS ZORN GMBH |
| Owner/operator number | 8010913 |
| Product codes | IOY |
| Device names | IOY - Support, Arm |
| Device class | Class I |
| Classification regulations (21 CFR) | 890.3475 |
| Review panels | Physical Medicine |
| Registered establishments | JULIUS ZORN GMBH, JULIUS ZORN, INC. |
| Establishment registrations | 2545, 1527846 |
| FEI numbers | 2545, 1527846 |
| 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