Home › Device types › FAD
Stent, Ureteral
FDA product code FAD · Class 2 · Gastroenterology, Urology
3,835
Registered devices
5,858
Adverse events
55
Recalls
122
510(k) clearances
Devices with this code
Contour VL™ — BOSTON SCIENTIFIC CORPORATIONBlack Silicone — COOK INCORPORATEDPorges Coloplast — Coloplast A/SUltrathane — COOK INCORPORATEDSof-Flex — COOK INCORPORATEDPolaris™ Ultra — BOSTON SCIENTIFIC CORPORATIONContour™ — BOSTON SCIENTIFIC CORPORATIONPolaris™ Loop — BOSTON SCIENTIFIC CORPORATIONPolaris™ Loop — BOSTON SCIENTIFIC CORPORATIONContour™ — BOSTON SCIENTIFIC CORPORATIONUniversa — COOK INCORPORATEDImaJin — Coloplast A/SUniversa — COOK INCORPORATEDPercuflex™ Plus — BOSTON SCIENTIFIC CORPORATIONQ UROLOGICAL PERSISTENT AGUAMEDICINA — Q UROLOGICAL CORPORATIONPercuflex™ Plus — BOSTON SCIENTIFIC CORPORATIONPolaris™ Loop — BOSTON SCIENTIFIC CORPORATIONDOUBLE-J — Gyrus ACMI, LLCSof-Flex — COOK INCORPORATEDPolaris™ Loop — BOSTON SCIENTIFIC CORPORATIONContour™ — BOSTON SCIENTIFIC CORPORATIONExpel™ Nephroureteral Stent System with Twist-Loc™ Hub — BOSTON SCIENTIFIC CORPORATIONPercuflex™ Plus — BOSTON SCIENTIFIC CORPORATIONContour™ — BOSTON SCIENTIFIC CORPORATION
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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