New Business Development, LLC is one of 21768 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
New Business Development, LLC - FDA 510(k) Cleared Devices
Recent clearances: PHENIX VERTEBRAL BODY REPLACEMENT, NBD HEAD SCREW, NBD DISPOSABLE RF CANNULAE
4
Total
3
Cleared
0
Denied
New Business Development, LLC has 3 FDA 510(k) cleared medical devices. Based in Woodstock, US.
Historical record: 3 cleared submissions from 2002 to 2007. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by New Business Development, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Spectra Medical Devices, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - New Business Development, LLC
4 devices