Proact L T D

FDA Filings

This page includes the latest FDA filings for Proact L T D. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number2183839
FEI Number2183839
NamePROACT, LTD.
Owner & OperatorPROACT, LTD.
Contact Address2452 General Potter Hwy. --
Centre Hall PA 16828 US
Official Correspondent
  • ALLAN J DARR
  • x-814-4048710-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address2452 General Potter Hwy.
Centre Hall, PA 16828 US
Establishment TypeDevelop Specifications But Do Not Manufacture At This Facility

FDA Owner/Operator Registration

FDA Filings

Device
Company
DeviceDate
PROACT, LTD.
Dynaflex2010-11-08
PROACT, LTD.
Quick Core II2007-11-28
PROACT, LTD.
Quick Core II2007-11-28
PROACT, LTD.
Quick Core I2007-11-28
PROACT, LTD.
Tal-Clip2007-11-28
PROACT, LTD.
QUICK CORE II1994-07-13
PROACT, LTD.
PROACT BIOPSY NEEDLE ENCHANCEMENTS1993-03-22
PROACT, LTD.
BONE-TEMNO/STERNUM-TEMNO1991-11-01
PROACT, LTD.
BAUER FLEXI-TEMNO BIOPSY NEEDLE1990-10-01
PROACT, LTD.
BAUER TEMNO BIOPSY NEEDLE1990-09-06

Similar & Related FDA Registered Companies

Related Finance Registrations
NCAGE Code0M2E5PROACT LTD
CAGE Code0M2E5PROACT LTD
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