Kiltex Corp

FDA Filings

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

FDA Registration(s)

• Registration Number: 1527493
• FEI Number: 1527493
• Name: KILTEX CORP.
• Owner & Operator: KILTEX CORP.
• Contact Address: 2064 KILLIAN RD. --; Akron OH 44312 US
• Official Correspondent:
  • TIMOTHY J KILLIAN
  • x-330-6446746-x
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: 2064 KILLIAN ROAD ; Akron, OH 44312 US
• Establishment Type:
  • Manufacture Medical Device
  • Manufacture Medical Device for Another Party (Contract Manufacturer)

FDA Filings

Device Company	Device	Date
GUDID 00859297006055 Kiltex Corporation	Kiltex Corporation	2018-07-23
GUDID 00859297006079 Kiltex Corporation	Kiltex Corporation	2018-07-06
GUDID 00859297006062 Kiltex Corporation	Kiltex Corpoartion	2018-07-06
GUDID 00859297006048 Kiltex Corporation	Kiltex Corporation	2018-07-06
GUDID 00859297006031 Kiltex Corporation	Kiltex Corporation	2018-07-06
GUDID 00859297006024 Kiltex Corporation	Kiltex Corporation	2018-07-06
GUDID 00859297006017 Kiltex Corporation	Kiltex Corporation	2018-07-06
GUDID 00859297006000 Kiltex Corporation	Kiltex Corporation	2018-07-06
PMN K070534 | HKY KILTEX CORP.	Tono Pen Probe Covers	2015-06-04
PMN K961029 | IYO KILTEX CORP.	Kiltex Probe Cover	2007-11-12
PMN K961029 KILTEX CORP.	KILTEX PROBE COVER	1996-07-25