FDA device listing
Juvent 1000
FDA device listing 1772305023 · Regenerative Technologies Corp dba Juvent
Key facts
| Proprietary names | Juvent 1000 |
|---|---|
| Owner/operator | Regenerative Technologies Corp dba Juvent |
| Owner/operator number | 10042771 |
| Product codes | BXB |
| Device names | BXB - Exerciser, Powered |
| Device class | Class I |
| Classification regulations (21 CFR) | 890.5380 |
| Review panels | Physical Medicine |
| Registered establishments | REGENERATIVE TECHNOLOGIES CORP dba JUVENT |
| Establishment registrations | 3010050274 |
| FEI numbers | 3010050274 |
| Establishment operations | Complaint File Establishment, 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