Arch Therapeutics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Arch Therapeutics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: AC5 Topical Gel, AC5 Topical Gel
2
Total
2
Cleared
0
Denied
Arch Therapeutics, Inc. has 2 FDA 510(k) cleared medical devices. Based in Framingham, US.
Historical record: 2 cleared submissions from 2018 to 2020. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Arch Therapeutics, Inc. Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Arch Therapeutics, Inc.
2 devices