Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3011253868

FEI Number

3011253868

Entity Name

PLENOPTIKA, INC.

City/State/Country

Cambridge, MA, US

Establishment Address

955 Massachusetts Ave, #339, Cambridge, MA 02139, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

PlenOptika, Inc (Owner Number: 10057539)

Owner / Operator Contact Address

955 Massachusetts Ave, #339, Cambridge, MA 02139, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HKO	Refractometer, Ophthalmic	Ophthalmic	Class 1	886.1760	2018-04-20

Official Correspondent

Shivang Dave

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

PlenOptika, Inc

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Similar Registrations

Registration Number	Establishment Name	Location
3023983572	PLENOPTIKA EUROPE SLU	Madrid Madrid (Province), ES
3008058416	View-M TECHNOLOGY CO., LTD	Gunpo-si Gyeonggi, KR
3013575858	APPASAMY ASSOCIATES PRIVATE LIMITED ( THIRUBHUVANAI))	Mannadipet Commune Puducherry, IN
1836161	ASPEN SURGICAL PRODUCTS, INC.	Caledonia, MI, US
3045062165	NINGBO FLO OPTICAL TECHNOLOGY DEVELOPMENT CO., LTD.	Ningbo Zhejiang, CN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3011253868. Last updated year: 2026. Please use registration number 3011253868 when referencing this establishment in official correspondence.