Keller Laboratories

FDA Filings

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

FDA Registration(s)

• Registration Number: 3006650414
• FEI Number: 3006650414
• Name: KELLER LABORATORIES
• Owner & Operator: National Dentex LLC
• Contact Address: 11601 Kew Garden Avenue, Suite 200 ; Palm Beach Gardens FL 33410 US
• Registration Status: 1
• Initial Importer: Y
• Registration Expiration: 2020-04-25
• Registration Address: 160 Larkin Williams Ind Ct ; Fenton, MO 63026 US
• Establishment Type:
  • Repack or Relabel Medical Device
  • Manufacture Medical Device for Another Party (Contract Manufacturer)
  • Manufacture Medical Device

FDA Filings

Device Company	Device	Date
PMN K133390 | LRK KELLER LABORATORIES [National Dentex LLC]	ClearDream	2016-12-13
NSP KELLER LABORATORIES [National Dentex LLC]	Restoration, porcelain	2013-03-06
NSL KELLER LABORATORIES [National Dentex LLC]	Full Dentures	2013-03-06
NSK KELLER LABORATORIES [National Dentex LLC]	Partial dentures	2013-03-06
PMN K971794 | LRK KELLER LABORATORIES [National Dentex LLC]	EMA	2012-12-12
PMN K062951 | LRK KELLER LABORATORIES [National Dentex LLC]	TAP Thornton Adjustable Positioner	2012-12-12
NSO KELLER LABORATORIES [National Dentex LLC]	porcelain fused to metal	2012-05-23
NSO KELLER LABORATORIES [National Dentex LLC]	pfm	2012-05-23

Similar & Related FDA Registered Companies

• KELLER LABORATORIES, INC.