ESCO Micro Pte. Ltd

FDA Device Registration & Listing · Singapore Central Singapore, SG · Registration 3008367374

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
3008367374
FEI Number
3008367374
Entity Name
ESCO Micro Pte. Ltd
City/State/Country
Singapore Central Singapore, SG
Establishment Address
21 Changi South Street 1, Singapore Central Singapore 486777, SG
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Esco Technologies Inc. or ETI (Owner Number: 10030836)
Owner / Operator Contact Address
903 Sheehy Drive, Horsham, PA 19044, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Esco

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LXG Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use Clinical Chemistry Class 1 862.2050 2013-02-01

Official Correspondent

No official correspondent registered.

US Agent Details

Barbara Hurst Business: Esco Technologies Email: barbara.hurst@escoglobal.com Phone: (215) 4419661

Related Public Records

Same Entity

Esco Technologies Inc. or ETI
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-0002-2008 Beckman Coulter Inc 1
FP1000 Cell Preparation System Software versions 1.1 & 1.2, Part Number 624922, for in vitro diagnostic use.
Z-0023-2013 Biomerieux Inc 1
PREVI Isola System, Catalog numbers 29500 and 29500R, bioMerieux, Inc., Durham, NC. Intended to perform the inoculation and streaking of Prepoured Media (PPM) with liquid microbiological samples.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008367374. Last updated year: 2026. Please use registration number 3008367374 when referencing this establishment in official correspondence.
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