Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3007034244

FEI Number

3007034244

Entity Name

Hi-Tech Mold Tool, Inc.

City/State/Country

Pittsfield, MA, US

Establishment Address

1 Technology Dr W, Pittsfield, MA 01201, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device

Owner / Operator

HI-TECH MOLD & TOOL, INC. (Owner Number: 10042779)

Owner / Operator Contact Address

1 Technology Drive West, Pittsfield, MA 01201, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Aptimax

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FSM	Tray, Surgical, Instrument	General, Plastic Surgery	Class 1	878.4800	2012-12-28

Official Correspondent

Paul Discoe

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

HI-TECH MOLD & TOOL, INC.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0027-2016	Zimmer, Inc.	1	Zimmer Universal Locking System, Titanium 3.5mm. Zimmer Implant and Instrument Cases are reusable, non-implantable devices designed to facilitate organization, identification, storage, transportation, cleaning, and sterilization processing of reusable instruments and certain unused implantable devices.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007034244. Last updated year: 2026. Please use registration number 3007034244 when referencing this establishment in official correspondence.