Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3016491661

FEI Number

3016491661

Entity Name

TITMUS LLC

City/State/Country

Fulton, MD, US

Establishment Address

11820 W Market Pl Ste K, Fulton, MD 20759, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Titmus LLC (Owner Number: 10062472)

Owner / Operator Contact Address

11820 West Market Place, Suite K, Fulton, MD 20759, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Titmus Titmus V3 Titmus V4 Titmus V2

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HQZ	Frame, Spectacle	Ophthalmic	Class 1	886.5842	2025-02-14
HIT	Tester, Color Vision	Ophthalmic	Class 1	886.1170	2020-01-31

Official Correspondent

Adam Zilberbaum

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Titmus LLC

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

Similar Registrations

Registration Number	Establishment Name	Location
3007521479	NY2LA INC.	Camarillo, CA, US
3005147601	VISIONTECH EXPORT INTERNATIONAL (PVT) LTD.	KARACHI Sindh, PK
3009554831	ROGER EYE DESIGN	Etten-Leur Noord-Brabant, NL
3013507321	DEM FACTORY S.R.L.	Limana Belluno, IT
3015243992	L.G.R SRL	Roma, IT

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3016491661. Last updated year: 2026. Please use registration number 3016491661 when referencing this establishment in official correspondence.