SYNPHNE PTE LTD

FDA Device Registration & Listing · Singapore South East, SG · Registration 3013517104

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
3013517104
FEI Number
3013517104
Entity Name
SYNPHNE PTE LTD
City/State/Country
Singapore South East, SG
Establishment Address
71 Bukit Batok Crescent, #08-02 Prestige Centre, Singapore South East 658071, SG
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Synphne Pte Ltd (Owner Number: 10054758)
Owner / Operator Contact Address
71 Bukit Batok Crescent,, #08-02 Prestige Centre, Singapore, SG-NOTA 658071, SG
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Synphne XPert

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HCC Device, Biofeedback Neurology Class 2 882.5050 2017-04-24

Official Correspondent

No official correspondent registered.

US Agent Details

Manoj Zacharias Business: Liberty Management Group Ltd. Email: office@libertymanagement.us Phone: (630) 2702921

Related Public Records

Same Entity

Synphne Pte Ltd
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K873418 Bodylog, Inc. BODYLOG STRESS REDUCTION PACKAGE 1987-12-17
K792659 Bio-Feedback Systems, Inc. FEEDBACK EDR SYSTEM MODEL ME-1 1980-01-09

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013517104. Last updated year: 2026. Please use registration number 3013517104 when referencing this establishment in official correspondence.
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