FDA device listing
Orthopedic Manual Surgical Instrument
FDA device listing 1019677696 · Medline ReNewal
Key facts
| Owner/operator | Medline ReNewal |
|---|---|
| Owner/operator number | 9033518 |
| 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 | Medline ReNewal |
| Establishment registrations | 3032391 |
| FEI numbers | 3002299608 |
| Establishment operations | Reprocessor of Single Use Devices |
| 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