Oertli Instrumente AG

FDA Regulatory Profile

Oertli Instrumente AG 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 Jun 27, 2024.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K233398Faros Surgical SystemJun 27, 2024
K133562CATARHEX 3Aug 12, 2014