ELSOHLY LABS, INC.

FDA Device Registration & Listing · OXFORD, MS, US · Registration 2319772

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
2319772
FEI Number
1000521247
Entity Name
ELSOHLY LABS, INC.
City/State/Country
OXFORD, MS, US
Establishment Address
5 INDUSTRIAL PARK DR., OXFORD, MS 38655, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
ELSOHLY LABS, INC. (Owner Number: 9019863)
Owner / Operator Contact Address
5 INDUSTRIAL PARK DR., --, OXFORD, MS 38655, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K951817
PMA Number
N/A

All Registered Proprietary Names

ELI Urine Controls

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
DIF Drug Mixture Control Materials Clinical Toxicology Class 1 862.3280 2007-12-07

Official Correspondent

MAHMOUD ELSOHLY, PH.D.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

ELSOHLY LABS, INC.
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
K803039 General Diagnostics PROFILE ANTI-CONVUL. SET ASSAYED S. CTL. 1980-12-22

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2319772. Last updated year: 2026. Please use registration number 2319772 when referencing this establishment in official correspondence.
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