Home › Device types › FAD
Stent, Ureteral
FDA product code FAD · Class 2 · Gastroenterology, Urology
3,837
Registered devices
5,967
Adverse events
55
Recalls
122
510(k) clearances
Devices with this code
Dornier MedTech — DORNIER MEDTECH AMERICA, INC.Q UROLOGICAL PERSISTENT AGUAMEDICINA — Q UROLOGICAL CORPORATIONBard® InLay® Ureteral Stent with NiCore™ Guidewire — C. R. Bard, Inc.Q UROLOGICAL FUSELAGE AGUAMEDICINA — Q UROLOGICAL CORPORATIONallSoft — ALLWIN MEDICAL DEVICES, INC.Polaris™ Loop — BOSTON SCIENTIFIC CORPORATIONImaJin — Coloplast A/SBard® InLay® Versa Fit® Ureteral Stent — C. R. Bard, Inc.Contour™ — BOSTON SCIENTIFIC CORPORATIONContour™ Injection Stent — BOSTON SCIENTIFIC CORPORATIONUniversa — COOK INCORPORATEDPercuflex™ Plus — BOSTON SCIENTIFIC CORPORATIONPercuflex™ Plus SureDrive™ — BOSTON SCIENTIFIC CORPORATIONPolaris™ Loop — BOSTON SCIENTIFIC CORPORATIONPercuflex™ Plus SureDrive™ — BOSTON SCIENTIFIC CORPORATIONPorges Coloplast — Coloplast A/SPorges Coloplast — Coloplast A/SSof-Flex — COOK INCORPORATEDBard® InLay Optima® Ureteral Stent — C. R. Bard, Inc.ImaJin — Coloplast A/SBlack Silicone — COOK INCORPORATEDAscerta™ — BOSTON SCIENTIFIC CORPORATIONPorges Coloplast — Coloplast A/SPorges Coloplast — Coloplast A/S
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-11-06 | C.R. Bard Inc | Labeling discrepancy; Ureteral stent actual size may not match the actual product label. |
| 2025-11-06 | C.R. Bard Inc | Labeling discrepancy; Ureteral stent actual size may not match the actual product label. |
| 2025-11-06 | C.R. Bard Inc | Labeling discrepancy; Ureteral stent actual size may not match the actual product label. |
| 2025-11-06 | C.R. Bard Inc | Labeling discrepancy; Ureteral stent actual size may not match the actual product label. |
| 2022-07-29 | Hobbs Medical, Inc. | Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9 |
| 2022-07-29 | Hobbs Medical, Inc. | Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9 |
| 2022-07-29 | Hobbs Medical, Inc. | Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9 |
| 2022-07-29 | Hobbs Medical, Inc. | Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9 |
| 2022-07-29 | Hobbs Medical, Inc. | Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9 |
| 2022-07-29 | Hobbs Medical, Inc. | Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9 |
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