Viscot Products Co., Ltd.

FDA Device Registration & Listing · Chbar Mon Kampong Speu, KH · Registration 3030228501

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
3030228501
FEI Number
3030228501
Entity Name
Viscot Products Co., Ltd.
City/State/Country
Chbar Mon Kampong Speu, KH
Establishment Address
Phum Samdach Ou, Khom Prey Nhiet, Srok, Chbar Mon Kampong Speu 050306, KH
Establishment Type(s)
Manufacture Medical Device,Export Device to the United States But Perform No Other Operation on Device
Owner / Operator
Wisdom Bright Pte Ltd. (Owner Number: 10091320)
Owner / Operator Contact Address
3 Raffles Place, 06-01 Bharat Building, Singapore, SG-01 048617, SG
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

MEDICINE AIRPLANE SPOON 1CT

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KYW Container, Liquid Medication, Graduated General Hospital Class 1 880.6430 2024-08-23

Official Correspondent

No official correspondent registered.

US Agent Details

Mindy McCann Email: USagent@Qservegroup.com Phone: (424) 2718169

Related Public Records

Same Entity

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

Similar Registrations

Registration Number Establishment Name Location
1000264713 GUPPY PLASTIC INDUSTRIES (PENANG) SDN BHD Bukit Mertajam, Penang Pulau Pinang, MY
3040185149 PT FOOD PACKAGING JAYA Indramayu Jawa Barat, ID
3015916830 PACKERMAN SDN. BHD. Melaka, MY
3010692406 SHANGHAI GUANGSHENG INDUSTRIAL CO.,LTD. Shanghai, CN
1423537 Cardinal Health 200, LLC Waukegan, IL, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3030228501. Last updated year: 2026. Please use registration number 3030228501 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.