Iogyn, Inc.

FDA Regulatory Profile

Iogyn, Inc. appears in FDA public data with 0 recalls, 3 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on August 29, 2014.

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K141848IOGYN SYSTEMAugust 29, 2014
DEN130040IOGYN SYSTEMMarch 28, 2014
K123330IOGYN ENDOSCOPEMarch 19, 2013