Pmbs, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pmbs, LLC - FDA 510(k) Cleared Devices
Recent clearances: MTS225 and MTS300 Multiple Tray Sterilization Systems
2
Total
2
Cleared
0
Denied
Pmbs, LLC has 2 FDA 510(k) cleared medical devices. Based in Stockton, US.
Historical record: 2 cleared submissions from 2015 to 2019. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Pmbs, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Hillring & Associates, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Pmbs, LLC
2 devices