Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3040937533

FEI Number

3040937533

Entity Name

MDD OPTIONS, LLC

City/State/Country

New Hill, NC, US

Establishment Address

355 Cedar Lane Farm Ln, New Hill, NC 27562, US

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198

Owner / Operator

MDD Options, LLC (Owner Number: 10094112)

Owner / Operator Contact Address

355 Cedar Lane Farm Ln, New Hill, NC 27562, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

FixOstar FixOstar - Hema MGG JetDye-AF System Kit Wright JetDye-AF JetBuffer pH 7.2 Wright-Giemsa JetDye-AF Kit Giemsa JetDye-AF MGG JetDye-AF Kit JaClean JetBuffer pH 6.8 JetBuffer pH 6.4 Wright-Giemsa JetDye-AF System Kit Wright-Giemsa JetDye-AF MG JetDye-AF Lugols JetDye-AF Safranin-FX JetDye-AF Gram-Polychrom JetDye-AF System Kit Methyleneblue JetDye-AF Crystal-Violete JetDye-AF Gram-Polychrom JetDye-AF Kit

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LED	Stains, Chemical Solution	Hematology	Class 1	864.1850	2026-04-24
GJL	Romanowsky Stains	Hematology	Class 1	864.1850	2026-04-24
JTS	Stains, Microbiologic	Hematology	Class 1	864.1850	2026-04-24

Official Correspondent

Adam Steadman

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

MDD Options, LLC

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

View Entity Profile →

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0025-05	Becton Dickinson & Co.	1	Difco (TM) BBL (TM) Gram Crystal Violet, 250 mL bottles in packs of four, catalog # 212525 and 3.8 L bottles, catalog # 212526, staining reagent.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3040937533. Last updated year: 2026. Please use registration number 3040937533 when referencing this establishment in official correspondence.