FDA device listing
Manual surgical instrument (all ranges)
FDA device listing 1450784752 · SPINEART SA
Key facts
| Proprietary names | Manual surgical instrument (all ranges) |
|---|---|
| Owner/operator | SPINEART SA |
| Owner/operator number | 10028947 |
| Product codes | LXH |
| Device names | LXH - Orthopedic Manual Surgical Instrument |
| Device class | Class I |
| Classification regulations (21 CFR) | 888.4540 |
| Review panels | Orthopedic |
| Registered establishments | ALPES CN SAS, SPINEART SA |
| Establishment registrations | 3007728266, 3037407500 |
| FEI numbers | 3007728266, 3037407500 |
| Establishment operations | Complaint File Establishment, Specification Developer, Contract Manufacturer, Foreign Exporter |
| 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