Kavo America Corporation

FDA Regulatory Profile

Kavo America Corporation appears in FDA public data with 0 recalls, 4 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on August 2, 2005.

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K042394DIAGNODENT PERIO TIP (ACCESSORY)August 2, 2005
K050744KAVO ERGOCOM/ERGOCAMApril 21, 2005
K042872RONDOFLEX PLUS 360November 23, 2004
K033221KAVO EVEREST ZH-BLANKOctober 28, 2003