Achaemenid, LLC

FDA Regulatory Profile

Achaemenid, LLC 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 August 25, 2026.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K254304iNOS intraoral biosensorAugust 25, 2026
K230532RADx Intraoral Appliance for Snoring and Sleep ApneaJuly 12, 2023