This page includes the latest FDA filings for Kobold. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
| Registration Number | 3009829958 |
| FEI Number | 3009829958 |
| Name | KOBOLD |
| Owner & Operator | Kobold LLC |
| Contact Address | 23403 E Mission Ave, Suite 220E Liberty Lake WA 99019 US |
| Official Correspondent |
|
| Registration Status | 1 |
| Initial Importer | N |
| Registration Expiration | 2020-04-25 |
| Registration Address | 23403 E Mission Ave Suite 220E Liberty Lake, WA 99019 US |
| Establishment Type | Complaint File Establishment per 21 CFR 820.198 |
Device Company | Device | Date |
|---|---|---|
KOBOLD [Kobold LLC] | Kobold? Prostate HDR Template(s) | 2017-07-12 |
KOBOLD [Kobold LLC] | Kobold? Prostate HDR Stepper Template(s) | 2017-07-12 |
KOBOLD [Kobold LLC] | Kobold? Interstitial Pencil Point Tip Stainless Steel Needle Set(s) - INACTIVE | 2017-07-12 |
KOBOLD [Kobold LLC] | Kobold? Interstitial Bevel Tip Stainless Steel Needle Set(s) - INACTIVE | 2017-07-12 |
KOBOLD [Kobold LLC] | Kobold? Vaginal Cylinder Applicator Set | 2017-07-12 |
KOBOLD [Kobold LLC] | Kobold? Miami Cylinder Applicator Set - INACTIVE | 2017-07-12 |
KOBOLD [Kobold LLC] | Kobold? Henschke-model Tandem and Ovoid Applicator Set | 2017-07-12 |
KOBOLD [Kobold LLC] | Kobold? Fletcher-model Tandem and Ovoid Applicator Set | 2017-07-12 |
KOBOLD [Kobold LLC] | Kobold Tandem and Ring Applicator Set | 2015-09-17 |