Home / Companies / Mani, Inc.

Mani, Inc.

FDA Regulatory Profile

Mani, Inc. appears in FDA public data with 0 recalls, 4 510(k) clearances, 0 FDA inspections, and 2 compliance actions on record. Its most recent 510(k) clearance was granted on May 19, 2006.

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
2

Recent 510(k) Clearances

K-NumberDeviceDate
K053638MANI NEEDLE & SUTURE PACK (SILK)May 19, 2006
K053637MANI NEEDLE & SUTURE PACK (NYLON)May 19, 2006
K053636MANI NEEDLE & SUTURE PACK (PGA ABSORBABLE)March 14, 2006
K050150MANI NEEDLE & SUTURE PACKDecember 5, 2005

FDA data resources