Aquilabs Us, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Aquilabs Us, LLC - FDA 510(k) Cleared Devices
Recent clearances: Hychloderm Wound and Skin Care (Rx) and Hychloderm Wound and Skin Care (OTC)
1
Total
1
Cleared
0
Denied
Aquilabs Us, LLC has 1 FDA 510(k) cleared medical devices. Based in Medley, US.
Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Aquilabs Us, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Aquilabs Us, LLC
1 devices