Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3014498538

FEI Number

3014498538

Entity Name

JINHUA CRAFTEK INSTRUMENT CO., LTD

City/State/Country

Jinhua Zhejiang, CN

Establishment Address

No. 500, Xian Hua North Street, Jinhua Zhejiang 321017, CN

Establishment Type(s)

Manufacture Medical Device,Export Device to the United States But Perform No Other Operation on Device

Owner / Operator

Jinhua Craftek Instrument Co., Ltd (Owner Number: 10057515)

Owner / Operator Contact Address

No. 500, Xian Hua North Street, Jinhua, CN-ZJ 321017, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Microtome Blade, CR75, CN80, CW75 Microtome, CR-701, CR-702, CR-703, CR-704, CR-705, CR-706, CR-801, CR-803, CR-905 Microtome, CR-601ST, CR-602, CR-603, CR-604, CR-605, CR-606 Water Bath, CR-210 Water Bath and Flattening table, CR-230A,CR-230B

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
IDL	Microtome, Accessories	Pathology	Class 1	864.3010	2018-04-18
IDY	Bath, Flotation, Tissue	Pathology	Class 1	864.3010	2018-04-18

Official Correspondent

Wenquan Zhou

US Agent Details

Mark Gordon Email: Mark.W.Gordon@outlook.com Phone: (571) 4072862

Related Public Records

Same Entity

Jinhua Craftek Instrument 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 3014498538. Last updated year: 2026. Please use registration number 3014498538 when referencing this establishment in official correspondence.