Sota Precision Optics, Inc. is one of 20549 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sota Precision Optics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: CLIO/CLIOSOFT, CLARIS I310D INTRAORAL CAMERA SYSTEM & ACCESSORIES, INTRA ORAL CAMERA SYSTEM AND ACCESSORIES, MODEL CLARIS I310
3
Total
3
Cleared
0
Denied
Sota Precision Optics, Inc. has 3 FDA 510(k) cleared medical devices. Based in Alpharetta, US.
Historical record: 3 cleared submissions from 2003 to 2011. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Sota Precision Optics, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.
FDA 510(k) Regulatory Record - Sota Precision Optics, Inc.
3 devices