Penner Manufacturing Inc

FDA Filings

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

FDA Registration(s)

• Registration Number: 1922538
• FEI Number: 1922538
• Name: PENNER MANUFACTURING INC
• Owner & Operator: PENNER MANUFACTURING, INC.
• Contact Address: 101 GRANT ST. ; Aurora NE 68818 US
• Official Correspondent:
  • Dean - Amundson
  • x-402-6945003-x
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: 101 Grant St ; Aurora, NE 68818 US
• Establishment Type: Manufacture Medical Device

FDA Filings

Device Company	Device	Date
PMN K040772 | ILJ PENNER MANUFACTURING INC [PENNER MANUFACTURING, INC.]	PACIFIC	2007-11-26
PMN K040772 PENNER MANUFACTURING, INC.	PACIFIC RECUMBENT HEIGHT-ADJUSTABLE BATH SYSTEM	2004-04-05
PMN K012061 PENNER MANUFACTURING, INC.	SUPERIOR BATH, MODEL 6300	2001-07-19
PMN K012057 PENNER MANUFACTURING, INC.	CASCADE BATH, MODEL 6900	2001-07-19