ESCO BIOENGINEERING

FDA Device Registration & Listing · Taichung, TW · Registration 3006571324

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3006571324
FEI Number
3006571324
Entity Name
ESCO BIOENGINEERING
City/State/Country
Taichung, TW
Establishment Address
36, 20th Road, Taichung Industrial Park, Taichung 40850, TW
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
esco bioengineering (Owner Number: 10087888)
Owner / Operator Contact Address
36, 20th Road, Taichung Industrial Park, Taichung, TW-NOTA 40850, TW
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

TideXcell CelXrocker BelloCell CelCradle X TideWave MiniTide CelCradle VXL Hybrid Bioreator CelCradle + TideCell CelCradle X Automated Cell Harvesting System TideXcell Automated Cell Harvesting System

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KJF System, Suspension, Cell Culture Hematology Class 1 864.2240 2023-04-26

Official Correspondent

king chang

US Agent Details

Zharmaine Solivet Business: Esco Technologies Inc Email: zharmaine.solivet@escolifesciences.com Phone: (215) 4419661

Related Public Records

Same Entity

esco bioengineering
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 3006571324. Last updated year: 2026. Please use registration number 3006571324 when referencing this establishment in official correspondence.
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