Sterizign Precision Technologies, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sterizign Precision Technologies, LLC - FDA 510(k) Cleared Devices
Recent clearances: SteriZign Signatur Device Protection System
1
Total
1
Cleared
0
Denied
Sterizign Precision Technologies, LLC has 1 FDA 510(k) cleared medical devices. Based in Brunswick, US.
Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Sterizign Precision Technologies, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Compliance Systems International, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Sterizign Precision Technologies, LLC
1 devices