Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3003915547

FEI Number

3003915547

Entity Name

PLASTINAX AUSTRAL LTD

City/State/Country

SAINT PIERRE Moka, MU

Establishment Address

INDUSTRIAL ZONE-MON DESERT, ALMA, SAINT PIERRE Moka --, MU

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

PLASTINAX AUSTRAL LTD (Owner Number: 9012465)

Owner / Operator Contact Address

INDUSTRIAL ZONE, MON DESERT ALMA, SAINT PIERRE, MU-NOTA 230, MU

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

CEBE Native Smith Costa Zeal HABER Quicksilver Honos Hobie

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HQZ	Frame, Spectacle	Ophthalmic	Class 1	886.5842	1995-02-16
HOI	Spectacle, Magnifying	Ophthalmic	Class 1	886.5840	1995-02-16

Official Correspondent

NICHOLAS PARK

US Agent Details

WRIGHT LISA Business: THE VISION COUNCIL Email: fda@thevisioncouncil.org Phone: (703) 5484560

Related Public Records

Same Entity

PLASTINAX AUSTRAL 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
K910951	United Optical, Spa	OPTHLAMIC FRAMES	1991-05-06

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3003915547. Last updated year: 2026. Please use registration number 3003915547 when referencing this establishment in official correspondence.