Reltus

FDA Filings

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

FDA Registration(s)

• Registration Number: 3009736760
• FEI Number: 3009736760
• Name: RELTUS
• Owner & Operator: Global Product Makers
• Contact Address: 1226 south Jordan parkway St D; South Jordan UT 84095 US
• Official Correspondent:
  • Matthew Hawkes
  • x-801-8359231-801
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: 1226 South Jordan Parkway Ste D; South Jordan, UT 84095 US
• Establishment Type: Manufacture Medical Device

FDA Filings

Device Company	Device	Date
MMD RELTUS [Global Product Makers]	Dr Blackwood	2019-09-11
KFZ RELTUS [Global Product Makers]	Mysture	2018-08-23
HQY RELTUS [Global Product Makers]	ooeye	2016-02-12
FTD RELTUS [Global Product Makers]	Warnock Medical	2015-01-12
FTD RELTUS [Global Product Makers]	Lumipen	2015-01-12
IRO RELTUS [Global Product Makers]	Reltus	2012-07-27
IRO RELTUS [Global Product Makers]	Myostorm	2012-07-27
IRO RELTUS [Global Product Makers]	Meteor	2012-07-27
IRO RELTUS [Global Product Makers]	Frejoi	2012-07-27