Eglobal, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Eglobal, LLC - FDA 510(k) Cleared Devices
Recent clearances: illumiflow 148 Laser Cap
2
Total
2
Cleared
0
Denied
Eglobal, LLC has 2 FDA 510(k) cleared medical devices. Based in Scottsdale, US.
Historical record: 2 cleared submissions from 2017 to 2018. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Eglobal, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Liza Burns and Associates as regulatory consultant.
FDA 510(k) Regulatory Record - Eglobal, LLC
2 devices