Accure Acne, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Accure Acne, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Accure Laser System, Accure Laser
2
Total
2
Cleared
0
Denied
Accure Acne, Inc. has 2 FDA 510(k) cleared medical devices. Based in Boulder, US.
Latest FDA clearance: Oct 2024. Active since 2022. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Accure Acne, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by FDA Compliance Group as regulatory consultant.
FDA 510(k) Regulatory Record - Accure Acne, Inc.
2 devices