Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3023983572

FEI Number

3023983572

Entity Name

PLENOPTIKA EUROPE SLU

City/State/Country

Madrid Madrid (Province), ES

Establishment Address

Calle Faraday 7, Office 2.06, Madrid Madrid (Province) 28049, ES

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

PLENOPTIKA EUROPE SLU (Owner Number: 10088304)

Owner / Operator Contact Address

Calle Faraday 7, Office 2.06, Madrid, ES-M 28049, ES

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

QuickSee Free Pro Keratometry QuickSee Free

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HKO	Refractometer, Ophthalmic	Ophthalmic	Class 1	886.1760	2023-06-27

Official Correspondent

Daryl Lim

US Agent Details

Shivang Dave Business: PLENOPTIKA, INC. Email: regulatory@plenoptika.com Phone: (617) 8632377

Related Public Records

Same Entity

PLENOPTIKA EUROPE SLU

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 3023983572. Last updated year: 2026. Please use registration number 3023983572 when referencing this establishment in official correspondence.