# Kobold, LLC

- Location (FDA's records): Liberty Lake, WA
- FDA decisions: 3 (2015–2017): 3 510(k) clearances
- Product codes: JAQ (3)
- Predicates its devices cite: 4 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Spencer Fillmore: 3 (https://510kreport.com/company/spencer-fillmore)
- Photon Technologies Corporation: 1 (https://510kreport.com/company/photon-technologies)

## Firms that cite its devices most
- Geomed Medizin-Technik GmbH & Co.: 1 (https://510kreport.com/company/geomed-medizin-technik)

## Its most-cited devices
- K170203: System, Applicator, Radionuclide, Remote Controlled (2017), cited by 1

## Recent decisions
- K170203: System, Applicator, Radionuclide, Remote Controlled (Jun 1, 2017)
- K160610: 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 (Feb 13, 2017)
- K142330: Kobold Ring and Tandem Applicator Set (Apr 9, 2015)

Source page: https://510kreport.com/company/kobold