Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3025308027

FEI Number

3025308027

Entity Name

BIOLENS LAB

City/State/Country

Mohammedia Mohammadia, MA

Establishment Address

Lot N 6 El Farah 2, Mohammedia Mohammadia 28810, MA

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Biolens Lab (Owner Number: 10086679)

Owner / Operator Contact Address

Lot N 6 El Farah 2, Mohammedia, MA-NOTA 28810, MA

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

BioSafty TPi4 BioSclere TPi1 BioSclere TP BioSclere TP1 BioSafty TP MSL BioSafty TPi BioSafty TP3 BioSclere TP4 BioSafty TPi3 BioSafty TE BioSclere MSL BioSafty MSP BioSclere TE MSL BioSclere TPi2 BioSafty MSL BioSclere TE MSP BioSafty TPO BioSclere TPi3 BioSafty TP MSP BioSclere TE BioSclere TPO BioSclere TP2 BioSclere MSP BioSclere BioSafty TP4 BioSafty TP1 BioSclere TP MSL BioSclere TPi4 BioSafty TP2 BioSclere TP MSP BioSafty TP BioSafty TPi1 BioSclere TP3 BioSafty BioSclere TPi BioSafty TPi2 BioFlex S2 TP BioK D BioK TP BioK D TP BioK D TI BioK BT BioFlex SA BT BioFlex S2 MSL BioFlex SA TP BioFlex S2 BT BioK TI BioK D MSL BioFlex SA BioK D BT BioK BioFlex SA TE BioK MSP BioFlex SA MSP BioFlex S2 TI BioK MSL BioK D TE BioFlex SA TI BioFlex S2 MSP BioFlex S2 BioFlex SA MSL BioFlex S2 TE BioK D MSP BioK TE BioSafty TPi1 BioFlex S2 TP BioSclere MSL BioSclere TP4 BioSafty TE BioSafty TP2 BioSclere TE MSP BioSclere TP MSL BioK D TI BioSclere TE MSL BioFlex S2 BioK D MSL BioFlex S2 BT BioSafty TP MSP BioSclere TP2 BioFlex SA BT BioFlex SA TP BioSafty MSP BioSafty TP4 BioFlex S2 TI BioSclere MSP BioFlex SA MSL BioK D TP BioSafty TPi4 BioSclere TPi1 BioK TE BioFlex SA TE BioSafty TP3 BioSclere TPi4 BioK TI BioK D BT BioSafty TPi2 BioFlex S2 MSL BioSclere TPO BioK D TE BioK TP BioSclere TP1 BioSclere BioK D MSP BioK BT BioSafty TP1 BioFlex SA MSP BioK MSP BioSclere TPi BioFlex S2 MSP BioSafty TPO BioSafty TP MSL BioSclere TP3 BioSclere TP BioSclere TPi2 BioSafty BioSclere TP MSP BioK MSL BioSafty TPi3 BioK D BioSafty MSL BioFlex SA TI BioFlex SA BioK BioSafty TP BioSafty TPi BioSclere TE BioSclere TPi3 BioFlex S2 TE OrthoLens TP OrthoLens

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HQD	Lens, Contact (Other Material) - Daily	Ophthalmic	Class 2	886.5916	2022-12-01
HQD	Lens, Contact (Other Material) - Daily	Ophthalmic	Class 2	886.5916	2022-12-01
HQD	Lens, Contact (Other Material) - Daily	Ophthalmic	Class 2	886.5916	2022-12-01
MUW	Lens, Contact (Orthokeratology)	Ophthalmic	Class 2	886.5916	2022-12-01

Official Correspondent

Mina Ziyani

US Agent Details

Bret Andre Business: EYEREG CONSULTING INC. Email: bandre@fdapproval.com Phone: (503) 3725226

Related Public Records

Same Entity

Biolens Lab

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
K963512	Benz Research and Development Corp.	BENZ B17 (KOLFOCON A) RIGID GAS PERMEABLE (HYDROPHOBIC DAILY WEAR CONTACT LENS (CLEAR AND TINTED, LATHE-CUT FROM LENS BL	1997-07-31

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3025308027. Last updated year: 2026. Please use registration number 3025308027 when referencing this establishment in official correspondence.