Armadillo Biomedical, LLC is one of 21689 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Armadillo Biomedical, LLC - FDA 510(k) Cleared Devices
Recent clearances: DacryoCATH, DACRYOCATH
2
Total
2
Cleared
0
Denied
Armadillo Biomedical, LLC has 2 FDA 510(k) cleared medical devices. Based in Irvine, US.
Historical record: 2 cleared submissions from 2012 to 2015. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Armadillo Biomedical, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Specialists, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Armadillo Biomedical, LLC
2 devices