Urosurge, Inc.

FDA Regulatory Profile

Urosurge, Inc. appears in FDA public data with 0 recalls, 4 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on February 9, 2000.

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
DEN000002UROSURGE PERCUTANEOUS SANS (STOLLER AFFERENT NERVE STIMULATOR) DEVICEFebruary 9, 2000
K992391UROSURGE SPIRALFLO URETERAL STENTAugust 18, 1999
K981491UROSURGE FILASTENT URETERAL STENTMay 29, 1998
K981489UROSURGE SPIRASTENT PLUS URETERAL STENTMay 29, 1998