Needle Specialty Products

FDA Filings

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

FDA Registration(s)

• Registration Number: 1000112137
• FEI Number: 1000112137
• Name: NEEDLE SPECIALTY PRODUCTS
• Owner & Operator: Needle Specialty Products
• Contact Address: 600 Highway 446 ; Boyle MS 38730 US
• Official Correspondent:
  • Gerald K Smith
  • x-662-8460640-225
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: 600 Highway 446 ; Boyle, MS 38730 US
• Establishment Type: Manufacture Medical Device for Another Party (Contract Manufacturer)

FDA Filings

Device Company	Device	Date
DTL NEEDLE SPECIALTY PRODUCTS	MAPs	2019-10-07
DRC NEEDLE SPECIALTY PRODUCTS	Majestik	2019-10-07
PMN K121092 | FPA NEEDLE SPECIALTY PRODUCTS	FlowEase Subcutaneous Infusion Set	2012-11-01
PMN K962077 | KNW NEEDLE SPECIALTY PRODUCTS	Biopty-Cut	2012-10-31
PMN K962077 | FCG NEEDLE SPECIALTY PRODUCTS	Biopty-Cut	2012-10-31
PMN K935457 | GDF NEEDLE SPECIALTY PRODUCTS	Dualok	2012-10-31
PMN K934370 | FCG NEEDLE SPECIALTY PRODUCTS	Magnum	2012-10-31
PMN K922939 | KNW NEEDLE SPECIALTY PRODUCTS	Maxcore	2012-10-31
PMN K915801 | GBX NEEDLE SPECIALTY PRODUCTS	Coaxial	2012-10-31
PMN K915801 | FCG NEEDLE SPECIALTY PRODUCTS	Coaxial	2012-10-31
PMN K910190 | KNW NEEDLE SPECIALTY PRODUCTS	Monopty	2012-10-31
PMN K910190 | KNW NEEDLE SPECIALTY PRODUCTS	Biopty-Cut	2012-10-31
GAB NEEDLE SPECIALTY PRODUCTS	Riza-Ribe Needle	2012-10-31
GAB NEEDLE SPECIALTY PRODUCTS	Granee Needle	2012-10-31