Kobold, LLC is one of 18890 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kobold, LLC - FDA 510(k) Cleared Devices
Recent clearances: System, Applicator, Radionuclide, Remote Controlled, Kobold Fletcher-model Tandem and Ovoid Applicator Set, Kobold Henschke-model Tandem and Ovoid Applicator Set, Kobold Vaginal Cylinder Applicator Set, Kobold Miami Cylinder Applicator Set, Kobold Ring and Tandem Applicator Set
3
Total
3
Cleared
0
Denied
Kobold, LLC has 3 FDA 510(k) cleared medical devices. Based in Liberty Lake, US.
Historical record: 3 cleared submissions from 2015 to 2017. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Kobold, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Bb Medical Surgical, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Kobold, LLC
3 devices