Proven Process Medical Devices Inc

FDA Filings

This page includes the latest FDA filings for Proven Process Medical Devices 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: 3003174284
• FEI Number: 3003174284
• Name: PROVEN PROCESS MEDICAL DEVICES, INC.
• Owner & Operator: PROVEN PROCESS MEDICAL DEVICES, INC.
• Contact Address: 110 FORBES BLVD. --; Mansfield MA 02048 US
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: 110 FORBES BLVD. ; MANSFIELD, MA 02048 US
• Establishment Type:
  • Sterilize Medical Device for Another Party (Contract Sterilizer)
  • Manufacture Medical Device for Another Party (Contract Manufacturer)

FDA Filings

Device Company	Device	Date
PMN P080012 | LKK PROVEN PROCESS MEDICAL DEVICES, INC.	Prometra	2013-01-31