SP MANUFACTURING PTE LTD

FDA Device Registration & Listing · Singapore Central Singapore, SG · Registration 3007740572

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
3007740572
FEI Number
3007740572
Entity Name
SP MANUFACTURING PTE LTD
City/State/Country
Singapore Central Singapore, SG
Establishment Address
25 Kallang Avenue #07-02, Singapore Central Singapore 339416, SG
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
SP Manufacturing Pte Ltd (Owner Number: 10029891)
Owner / Operator Contact Address
25 Kallang Avenue #07-02, Singapore, SG-01 339416, SG
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

SUJI Gen 2, SUJI PRO

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
QGX General Use Pneumatic Tourniquet General, Plastic Surgery Class 1 878.5910 2024-02-28

Official Correspondent

Jenny Sim

US Agent Details

Edwin Lindsay Email: edwin@rafsolutions.net Phone: (305) 9607262

Related Public Records

Same Entity

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

Other Registrations for Same Entity

Registration Number Establishment Name Location
3011842549 PT. SP Manufacturing Batam Riau, ID

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007740572. Last updated year: 2026. Please use registration number 3007740572 when referencing this establishment in official correspondence.
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