Kiierr International, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kiierr International, LLC - FDA 510(k) Cleared Devices
Recent clearances: Kiierr 272 Laser, Kiierr 148 Laser
1
Total
1
Cleared
0
Denied
Kiierr International, LLC has 1 FDA 510(k) cleared medical devices. Based in Salt Lake City, US.
Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Kiierr International, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Nst Consultants, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Kiierr International, LLC
1 devices