Achaemenid, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Achaemenid, LLC - FDA 510(k) Cleared Devices
Recent clearances: RADx Intraoral Appliance for Snoring and Sleep Apnea
1
Total
1
Cleared
0
Denied
Achaemenid, LLC has 1 FDA 510(k) cleared medical devices. Based in Stratford, US.
Last cleared in 2023. Active since 2023. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Achaemenid, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Aztech Regulatory & Quality, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Achaemenid, LLC
1 devices