Nuortho Surgical, Inc. is one of 22321 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Nuortho Surgical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: CERULEAU ELECTROSURGICAL PROBE
1
Total
1
Cleared
0
Denied
Nuortho Surgical, Inc. has 1 FDA 510(k) cleared medical devices. Based in Newington, US.
Historical record: 1 cleared submissions from 2010 to 2010. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Nuortho Surgical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Nuortho Surgical, Inc.
1 devices