FDA device listing
Lifenet2559 (WH,CH1*) - Dual Link,Lifenet2559 (WH,CH1*) - FlexiGRAFT Connect; FlexiGRAFT Connect EXT,Lifenet2559…
FDA device listing 1172175355 · STERIS Corporation
Key facts
| Proprietary names | Lifenet2559 (WH,CH1*) - Dual Link,Lifenet2559 (WH,CH1*) - FlexiGRAFT Connect; FlexiGRAFT Connect EXT,Lifenet2559 (WH,CH1*) - FlexiGRAFT GraftLink; FlexiGRAFT GraftLink TS,Lifenet2559 (WH,CH1*) - FlexiGRAFT QuadLink,Lifenet2559 (WH,CH1*) - FlexiGRAFT Sutured Lateral Ankle Tendon Construct |
|---|---|
| Owner/operator | STERIS Corporation |
| Owner/operator number | 1527821 |
| Product codes | GAT |
| Device names | GAT - Suture, Nonabsorbable, Synthetic, Polyethylene |
| Device class | Class II |
| Classification regulations (21 CFR) | 878.5000 |
| Review panels | General & Plastic Surgery |
| Registered establishments | ISOMEDIX OPERATIONS INC. |
| Establishment registrations | 1319660, 2245304 |
| FEI numbers | 2245304, 1000136478 |
| Establishment operations | Contract Sterilizer |
| 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