MedtechSourcebook

Hi-Tech Mold Tool, Inc.

Contract manufacturer ยท Pittsfield, MA

FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified

2012Product codes first listed, by year (tallest: 1)2026
FDA registration
3007034244 (openFDA record; or search FDA's registration database)
FEI number
3007034244
Registered for
FDA registration year 2026
Establishment types
Manufacturer; Contract manufacturer
Owner or operator
HI-TECH MOLD & TOOL, INC. (FDA owner/operator no. 10042779)
Registered address
1 Technology Dr W, Pittsfield, MA 01201
Contract listings
2 device listings, 2 product codes, first listed Dec 28, 2012
Certification
Not verified. We have no certification data for this facility yet.

Devices listed as contract work

Each row is an FDA product code this facility lists under its contract establishment type, with the date of its earliest such listing.

Product codeDevice (FDA name)ClassCategoryRoleFirst listed
FRGWrap, SterilizationClass IIGeneral hospitalContract manufacturingJan 11, 2013
FSMTray, Surgical, InstrumentClass IGeneral and plastic surgeryContract manufacturingDec 28, 2012