D K Technologies G M B H

FDA Filings

This page includes the latest FDA filings for D K Technologies G M B H. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3004059738
FEI Number3004059738
NameKirby Rust
Owner & OperatorD&K TECHNOLOGIES GMBH
Contact Address7/8 KANALWEG --
BARUM DE-NOTA 21357 DE
Official Correspondent
  • PETER - KLEWS
  • 049-4133-510185-x
US Agent
Importing Logistics Registration
ImporterTrod Medical
Address11045 Gatewood Dr.
Bradenton, FL 34211 UNITED STATES
Importer TypeRetailer
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address5588 Benton Woods Drive
ATL, GA 30342 US
Establishment Type
  • Develop Specifications But Do Not Manufacture At This Facility
  • Manufacture Medical Device

FDA Filings

Device
Company
DeviceDate
Kirby Rust [D&K TECHNOLOGIES GMBH]
Image Plus2010-06-09
Kirby Rust [D&K TECHNOLOGIES GMBH]
WOLF ENDOMOTION SYSTEM2004-04-02
Kirby Rust [D&K TECHNOLOGIES GMBH]
TargetPro Needle Holder2004-04-02
Kirby Rust [D&K TECHNOLOGIES GMBH]
Template Fixation Applicator2003-05-30
Kirby Rust [D&K TECHNOLOGIES GMBH]
Template Applicator2003-05-30
Kirby Rust [D&K TECHNOLOGIES GMBH]
SOLIDLOCK POSITIONING2003-05-30
Kirby Rust [D&K TECHNOLOGIES GMBH]
Disposable Template Grid 18G2003-05-30

Related Finance Registrations
NCAGE CodeCC750D&K TECHNOLOGIES GMBH
CAGE CodeCC750D&K TECHNOLOGIES GMBH
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