Tissue-Tek Xpress®

x120 Rapid Tissue Processor

Registry build 21.09.26
5manufacturers in China registered for this device type
3catalogue numbers in this listing
1510(k) clearance

Who Else Makes It

Concentrated in Guangdong (2), Hunan (1), Shanghai (1).

Chinese manufacturers registered for FDA product code IEO
Manufacturer City Province Registered as Device types
Guangzhou Four E’s Scientific Co., Ltd. Guangzhou Guangdong Contract manufacturer 61
AVE Science & Technology Co., Ltd. Changsha Hunan Manufacturer 22
Leica Instruments (Shanghai) Co., Ltd. Shanghai Shanghai Contract manufacturer 11
Dakewe(Shenzhen) Medical Equipment Co., Ltd. Shenzhen Guangdong Repacker / relabeller 9
Hangzhou Healthsky Biotechnology Co., Ltd. Hangzhou Zhejiang Manufacturer 6

Record

Regulatory record for Tissue-Tek Xpress®
Listed by Sakura Finetek U.S.A., Inc., United States
FDA product code IEO
Device type Processor, Tissue, Automated
Device class Class 1
Regulation 21 CFR 864.3875
Establishment Specification developer, Complaint-file establishment, Manufacturer
Premarket notification Exempt
Record published 2020-05-06
Record revised 2022-09-16 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Label carries manufacturing date, serial number
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Tissue-Tek Xpress®
Catalogue number Size Status
7750 In distribution
7109 In distribution
7720 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Epredia Shandon Diagnostics Limited 25
Thermo Fisher Shandon Diagnostics Limited 11
HistoCore Peloris Leica Biosystems Melbourne PTY Ltd 9
Tissue-Tek VIP® 6 Sakura Finetek U.S.A., Inc. 2
PathTezt® Biocytech Corporation SDN BHD 2
Tissue-Tek VIP® Sakura Finetek U.S.A., Inc. 2
Basket Leica Biosystems Nussloch Gmbh 1
Basket, assy., large Leica Biosystems Nussloch Gmbh 1
Anybattery Anybattery, Inc 1
Leica ASP300 S Leica Biosystems Nussloch Gmbh 1
HistoPro® Rushabh Instruments, LLC 1
ASP6025 China Leica Biosystems Nussloch Gmbh 1

Showing 12 of 52. All products under Processor, Tissue, Automated

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K881165 1988-07-01

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer