FDA device listing
MOB1025 3-Wheel Mobility Scooter,MOB1027 4-Wheel Mobility Scooter,MOB1030 Folding Mobility Scooter,MOB1053 Mobility…
FDA device listing 1619009189 · VIVE Health LLC
Key facts
| Proprietary names | MOB1025 3-Wheel Mobility Scooter,MOB1027 4-Wheel Mobility Scooter,MOB1030 Folding Mobility Scooter,MOB1053 Mobility Scooter - Series A |
|---|---|
| Owner/operator | VIVE Health LLC |
| Owner/operator number | 10047487 |
| Premarket submissions | K062645 |
| Product codes | INI |
| Device names | INI - Vehicle, Motorized 3-Wheeled |
| Device class | Class II |
| Classification regulations (21 CFR) | 890.3800 |
| Review panels | Physical Medicine |
| Registered establishments | VIVE Health LLC |
| Establishment registrations | 3011191255 |
| FEI numbers | 3011191255 |
| Establishment operations | Repackager/Relabeler |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 1–9 UDI devices (GUDID) under the same submission
- 1–9 Device listings citing the same submission
- Yes 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