Ankon Technologies Co., Ltd.

FDA Regulatory Profile

Ankon Technologies Co., Ltd. appears in FDA public data with 0 recalls, 2 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on December 12, 2023.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
DEN230027NaviCam ProScanDecember 12, 2023
K221590NaviCam Small Bowel Capsule Endoscopy SystemDecember 2, 2022