Home › Device types › DYF
Prosthesis, Vascular Graft, Of Less Then 6mm Diameter
FDA product code DYF · Class 2 · Cardiovascular
491
Registered devices
196
Adverse events
17
Recalls
21
510(k) clearances
Devices with this code
GORE ACUSEAL Vascular Graft — W. L. Gore & Associates, Inc.IMPRA® ePTFE Vascular Grafts — Bard Peripheral Vascular, Inc.IMPRA® ePTFE Vascular Grafts — Bard Peripheral Vascular, Inc.ADVANTA SLIDER GDS — Atrium Medical CorporationIMPRA® ePTFE Vascular Grafts — Bard Peripheral Vascular, Inc.MAXIFLO™ — VASCUTEK LTDGORE PROPATEN Vascular Graft — W. L. Gore & Associates, Inc.IMPRA® ePTFE Vascular Grafts — Bard Peripheral Vascular, Inc.IMPRA® ePTFE Vascular Grafts — Bard Peripheral Vascular, Inc.IMPRA® ePTFE Vascular Grafts — Bard Peripheral Vascular, Inc.GORE-TEX Vascular Graft — W. L. Gore & Associates, Inc.IMPRA® ePTFE Vascular Grafts — Bard Peripheral Vascular, Inc.IMPRA® ePTFE Vascular Grafts — Bard Peripheral Vascular, Inc.GORE PROPATEN Vascular Graft — W. L. Gore & Associates, Inc.IMPRA® ePTFE Vascular Grafts — Bard Peripheral Vascular, Inc.IMPRA® ePTFE Vascular Grafts — Bard Peripheral Vascular, Inc.IMPRA® ePTFE Vascular Grafts — Bard Peripheral Vascular, Inc.IMPRA® ePTFE Vascular Grafts — Bard Peripheral Vascular, Inc.IMPRA® ePTFE Vascular Grafts — Bard Peripheral Vascular, Inc.VECTRA®, VASCULAR ACCESS GRAFT — Thoratec CorporationDistaflo® Bypass Grafts — Bard Peripheral Vascular, Inc.exGraft — PECA LABS, INC.IMPRA® ePTFE Vascular Grafts — Bard Peripheral Vascular, Inc.IMPRA® ePTFE Vascular Grafts — Bard Peripheral Vascular, Inc.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-05-03 | Atrium Medical Corporation | Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces. |
| 2024-05-03 | Atrium Medical Corporation | Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces. |
| 2024-05-03 | Atrium Medical Corporation | Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces. |
| 2024-05-03 | Atrium Medical Corporation | Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces. |
| 2024-05-03 | Atrium Medical Corporation | Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces. |
| 2024-05-03 | Atrium Medical Corporation | Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces. |
| 2024-05-03 | Atrium Medical Corporation | Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces. |
| 2024-05-03 | Atrium Medical Corporation | Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces. |
| 2024-05-03 | Atrium Medical Corporation | Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces. |
| 2024-05-03 | Atrium Medical Corporation | Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.