Pinyons Medical Technology, Inc. is one of 25152 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pinyons Medical Technology, Inc. - FDA 510(k) Cleared Devices
Recent clearances: POWRSYRINGE ASPIRATOR, POWRSYRINGE INJECTOR, POWRSYRINGE MONITOR
3
Total
3
Cleared
0
Denied
Pinyons Medical Technology, Inc. has 3 FDA 510(k) cleared medical devices. Based in Park City, US.
Historical record: 3 cleared submissions from 2007 to 2007. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Pinyons Medical Technology, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Pinyons Medical Technology, Inc.
3 devices