ARTICARES PTE LTD

FDA Device Registration & Listing · SINGAPORE Central Singapore, SG · Registration 3029906445

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
3029906445
FEI Number
3029906445
Entity Name
ARTICARES PTE LTD
City/State/Country
SINGAPORE Central Singapore, SG
Establishment Address
67 Ayer Rajah Crescent, #07-11 12 Singapore 139950, SINGAPORE Central Singapore 139950, SG
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Articares Pte Ltd (Owner Number: 10087472)
Owner / Operator Contact Address
67 Ayer Rajah Crescent, #07-11/12, SINGAPORE, SG-01 139950, SG
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

ReHandyBot V1 H-MAN V1

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IKK System, Isokinetic Testing And Evaluation Physical Medicine Class 2 890.1925 2023-10-02

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

Articares Pte Ltd
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 3029906445. Last updated year: 2026. Please use registration number 3029906445 when referencing this establishment in official correspondence.
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