FDA device listing
PERI-STRIPS Dry Staple Line Reinforcement with VERITAS Collagen Matrix with SECURE GRIP Technology
FDA device listing 1380191814 · BAXTER HEALTHCARE CORPORATION
Key facts
| Proprietary names | PERI-STRIPS Dry Staple Line Reinforcement with VERITAS Collagen Matrix with SECURE GRIP Technology |
|---|---|
| Owner/operator | BAXTER HEALTHCARE CORPORATION |
| Owner/operator number | 1417572 |
| Premarket submissions | K213125 |
| Product codes | FTM, OXE |
| Device names | FTM - Mesh, Surgical, OXE - Mesh, Surgical, Collagen, Staple Line Reinforcement |
| Device class | Class II |
| Classification regulations (21 CFR) | 878.3300 |
| Review panels | General & Plastic Surgery |
| Registered establishments | BAXTER HEALTHCARE CORPORATION, SYNOVIS LIFE TECHNOLOGIES, INC. (A Subsidiary of Baxter International Inc.) |
| Establishment registrations | 1416980, 2183620 |
| FEI numbers | 1416980, 2183620 |
| Establishment operations | Complaint File Establishment, Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 1–9 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