Kirby Rust

FDA Filings

This page includes the latest FDA filings for Kirby Rust. 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

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