Surgical Direct, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Surgical Direct, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Surgical Direct Hand-held Laparoscopic Instruments
1
Total
1
Cleared
0
Denied
Surgical Direct, Inc. has 1 FDA 510(k) cleared medical devices. Based in Deland, US.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Surgical Direct, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Smith Associates as regulatory consultant.
FDA 510(k) Regulatory Record - Surgical Direct, Inc.
1 devices