Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3027396409

FEI Number

3027396409

Entity Name

123 SEE

City/State/Country

Boston, MA, US

Establishment Address

240 Commercial Street, 3A, Boston, MA 02109, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

123 SEE (Owner Number: 10088135)

Owner / Operator Contact Address

240 Commercial Street, 3A, Boston, MA 02109, 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
QTO	Digital Visual Acuity Test	Ophthalmic	Class 1	886.1150	2023-05-31
HKO	Refractometer, Ophthalmic	Ophthalmic	Class 1	886.1760	2023-05-31
HLM	Instrument, Measuring, Lens, Ac-Powered	Ophthalmic	Class 1	886.1425	2023-05-31

Official Correspondent

Matthias Hofmann

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

123 SEE

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 3027396409. Last updated year: 2026. Please use registration number 3027396409 when referencing this establishment in official correspondence.