Hi Tech Mold Tool Inc

FDA Filings

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

FDA Registration(s)
Registration Number3007034244
FEI Number3007034244
NameHi-Tech Mold Tool, Inc.
Owner & OperatorHI-TECH MOLD & TOOL, INC.
Contact Address1 Technology Drive West
Pittsfield MA 01201 US
Official Correspondent
  • Paul D Discoe
  • x-413-4439184-413
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address1 Technology Dr W
Pittsfield, MA 01201 US
Establishment Type
  • Manufacture Medical Device
  • Manufacture Medical Device for Another Party (Contract Manufacturer)

FDA Filings

Device
Company
DeviceDate
Hi-Tech Mold Tool, Inc. [HI-TECH MOLD & TOOL, INC.]
Aptimax Tray System2013-01-11
Hi-Tech Mold Tool, Inc. [HI-TECH MOLD & TOOL, INC.]
Aptimax2012-12-28

Related Finance Registrations
NCAGE Code3MSQ2HI-TECH MOLD & TOOL INC.
CAGE Code3MSQ2HI-TECH MOLD & TOOL, INC.
DUNS101291219HI-TECH MOLD & TOOL, INC.
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