Geneoscopy, Inc.

FDA Regulatory Profile

Geneoscopy, Inc. appears in FDA public data with 1 recall, 0 510(k) clearances, 2 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-2077-2025, Class II) was initiated on May 20, 2025.

Summary

Total Recalls
1
510(k) Clearances
0
Inspections
2
Compliance Actions
0

Recent Recalls

NumberClassProductDate
Z-2077-2025Class IIColoSense Test Kit, Part No. 80-001, component of ColoSense testMay 20, 2025