Kohlbrat Bunz

FDA Filings

This page includes the latest FDA filings for Kohlbrat Bunz. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3005588647
FEI Number3005588647
NameKOHLBRAT & BUNZ
Owner & OperatorDomico Med-Device
Contact Address14241 N. Fenton RD
Fenton MI 48430 US
Official Correspondent
  • Domico Med-Device
  • 1-810-7505300-5359
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration AddressLoretostrasse 4-8
Radstadt Salzburg, 5550 AT
Establishment Type
  • Manufacture Medical Device for Another Party (Contract Manufacturer)
  • Manufacture Medical Device

FDA Filings

Device
Company
DeviceDate
KOHLBRAT & BUNZ [Domico Med-Device]
Arm splints; Child splints; Dual leg splints; Hand, Foot, Wrist, Ankle, Leg Splints; Head splints; Infant Splints2018-05-29

Related Finance Registrations
NCAGE Code01CK3KOHLBRAT AND BUNZ
CAGE Code01CK3KOHLBRAT AND BUNZ
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