Arobella Medical, LLC is one of 19699 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Arobella Medical, LLC - FDA 510(k) Cleared Devices
Recent clearances: AR1000 SERIES ULTRASONIC WOUND THERAPY SYSTEM, AS 1000 ULTRASOUND WOUND THERAPY SYSTEM, AR1000 ULTRASONIC WOUND THERAPY SYSTEM
3
Total
3
Cleared
0
Denied
Arobella Medical, LLC has 3 FDA 510(k) cleared medical devices. Based in Carmel, US.
Historical record: 3 cleared submissions from 2007 to 2014. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Arobella Medical, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Arobella Medical, LLC
3 devices