OLYLIFE INTERNATIONAL SDN BHD

FDA Device Registration & Listing · Wilayah Persekutuan Kuala Lumpur, MY · Registration 3027436335

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
3027436335
FEI Number
3027436335
Entity Name
OLYLIFE INTERNATIONAL SDN BHD
City/State/Country
Wilayah Persekutuan Kuala Lumpur, MY
Establishment Address
BO-01, LG, L1 & L7, BLOCK 1, SOUTHBANK COMMERCIAL, PUSAT KOMMSIAL TEBING SELATAN, NO.179, JALAN KLANG LAMA, Wilayah Persekutuan Kuala Lumpur 58000, MY
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
OLYLIFE INTERNATIONAL SDN BHD (Owner Number: 10088116)
Owner / Operator Contact Address
BO-01, LG, L1 & L7, BLOCK 1, SOUTHBANK COMMERCIAL, PUSAT KOMMSIAL TEBING SELATAN, NO.179, JALAN KLANG LAMA, Wilayah Persekutuan, MY-14 58000, MY
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Floating Natural Bamboo Fiber Sanitary Pads – Gift Set SL-6 OLYLIFE Shaken Massager SK-M3 OLYLIFE THz Tera-P90+, Model: P90+

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HHD Pad, Menstrual, Unscented Obstetrics/Gynecology Class 1 884.5435 2025-08-05
ISA Massager, Therapeutic, Electric Physical Medicine Class 1 890.5660 2024-03-27

Official Correspondent

HUI LEE

US Agent Details

Levi Lee Email: 2300908048@qq.com Phone: (408) 9809679

Related Public Records

Same Entity

OLYLIFE INTERNATIONAL SDN BHD
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
K823241 Kimberly-Clark Corp. NEW FREEDOM THIN UNSCENTED MAXI PADS 1982-12-28

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3027436335. Last updated year: 2026. Please use registration number 3027436335 when referencing this establishment in official correspondence.
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