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Ureteral Stent Company

FDA Regulatory Profile

Ureteral Stent Company appears in FDA public data with 0 recalls, 2 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on March 22, 2024.

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Known Names

ureteral stent, ureteral stent company

Recent 510(k) Clearances

K-NumberDeviceDate
K232920RELIEF™ Ureteral Stent Kit; Model: RS-001 - 6 Fr x 24cm, RELIEF™ Ureteral Stent Kit; Model: RS-002 -March 22, 2024
K213444RELIEF Ureteral Stent Kit; Model: RS-001 - 6 Fr x 24cm, RELIEF Ureteral Stent Kit; Model: RS-002 - 6March 17, 2022

FDA data resources