Spectra, Inc. is one of 24671 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Spectra, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SPECTRA MEDICAL SAFETY SCAPEL
1
Total
1
Cleared
0
Denied
Spectra, Inc. has 1 FDA 510(k) cleared medical devices. Based in Wilmington, US.
Historical record: 1 cleared submissions from 2009 to 2009. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Spectra, Inc. 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 - Spectra, Inc.
1 devices