FDA device listing
Guide, Drill, Ligament
FDA device listing 2012111779 · ARTHREX, INC.
Key facts
| Owner/operator | ARTHREX, INC. |
|---|---|
| Owner/operator number | 1220287 |
| Product codes | LXI |
| Device names | LXI - Guide, Drill, Ligament |
| Device class | Class I |
| Classification regulations (21 CFR) | 878.4820 |
| Review panels | General & Plastic Surgery |
| Registered establishments | Arthrex Distribution Hub EMEA B.V., Arthrex do Brazil Importacao e Comercio de Equipamentos Medicos Ltda, Arthrex GmbH, Arthrex, Inc., ARTHREX, INC., Arthrex Japan G.K. (Shinjuku), Arthrex Manufacturing Inc., Arthrex (Shanghai) Co., Ltd., Arthrex Singapore Pte Ltd. |
| Establishment registrations | 1220246, 3002579136, 3010331645, 3012470322, 3014004349, 3014262693, 3015231789, 3015974593, 3016851379 |
| FEI numbers | 1220246, 3002579136, 3010331645, 3012470322, 3014004349, 3014262693, 3015231789, 3015974593, 3016851379 |
| Establishment operations | Contract Manufacturer, Contract Sterilizer, Foreign Exporter, Specification Developer |
| 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