Spiraltech Superior Dental Implants, Inc. is one of 18461 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Spiraltech Superior Dental Implants, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SpiralTech Dental Implant System
1
Total
1
Cleared
0
Denied
Spiraltech Superior Dental Implants, Inc. has 1 FDA 510(k) cleared medical devices. Based in Chicago, US.
Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Spiraltech Superior Dental Implants, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Blackwell Device Consulting as regulatory consultant.
FDA 510(k) Regulatory Record - Spiraltech Superior Dental Implants, Inc.
1 devices