Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3004362293

FEI Number

3004362293

Entity Name

CROSSTECH DIAMOND TOOLS CO., LTD.

City/State/Country

Samutprakran Samut Prakan, TH

Establishment Address

109/87 MOO 2 TEPARAK ROAD, SAMUTPRAKRAN, Samutprakran Samut Prakan 10540, TH

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

CROSSTECH DIAMOND TOOLS CO., LTD. (Owner Number: 9059968)

Owner / Operator Contact Address

109/87 MOO 2 TEPARAK ROAD, SAMUTPRAKRAN, BANGSAOTHONG, TH-NOTA 10540, TH

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Crosstech

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
EJL	Bur, Dental	Dental	Class 1	872.3240	2003-12-03

Official Correspondent

No official correspondent registered.

US Agent Details

Linda Laine Business: DENTALREE.COM INTERNATIONAL Email: linda0laine@gmail.com Phone: (408) 4552150

Related Public Records

Same Entity

CROSSTECH DIAMOND TOOLS CO., LTD.

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

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004362293. Last updated year: 2026. Please use registration number 3004362293 when referencing this establishment in official correspondence.