FDA device listing
Vertebral Body Tethering System
FDA device listing 1948135611 · Highridge Medical, LLC
Key facts
| Owner/operator | Highridge Medical, LLC |
|---|---|
| Owner/operator number | 9061535 |
| Premarket submissions | H190005 |
| Product codes | QHP |
| Device names | QHP - Vertebral Body Tethering System |
| Device class | Not classified |
| Classification regulations (21 CFR) | ORCA1.QHP |
| Review panels | Orthopedic |
| Registered establishments | Highridge Medical, LLC, Olive Branch Distribution Center |
| Establishment registrations | 3012447612, 3016050940 |
| FEI numbers | 3012447612, 3016050940 |
| Establishment operations | Contract Manufacturer, Specification Developer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 10–99 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