INCELL CORPORATION, LLC

FDA Device Registration & Listing · SAN ANTONIO, TX, US · Registration 3004107906

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
3004107906
FEI Number
3004107906
Entity Name
INCELL CORPORATION, LLC
City/State/Country
SAN ANTONIO, TX, US
Establishment Address
12734 CIMARRON PATH, SAN ANTONIO, TX 78249, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
INCELL CORPORATION, LLC (Owner Number: 9057577)
Owner / Operator Contact Address
12734 CIMARRON PATH, San Antonio, TX 78249, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

SMX-XF ZAPR ZSOL:F M4:BaseA ZTM:A1 M3:BaseF M3:BaseA ZTM:A2 EZ-CPZ M3:10A EZ-CPZ-ND+2% Hetastarch EZ-CPZ-ND:pL2 EZ-CPZ:pL2 EZ-CPZ:Y25 EZ-CPZ-ND M4:BaseF M3:DC EZ-CPZ-ND:Y25 ZEFR

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
JSK Supplement, Culture Media Microbiology Class 1 866.2450 2003-07-23
GGK Products, Red-Cell Lysing Products Hematology Class 1 864.8540 2023-08-30
KIP Formulations, Balanced Salt Solutions Hematology Class 1 864.2875 2023-08-30
KIT Media And Components, Synthetic Cell And Tissue Culture Hematology Class 1 864.2220 2003-07-23

Official Correspondent

MARY PAT MOYER, PH.D.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

INCELL CORPORATION, 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
K832690 Sigma Chemical Co. MINIMUM ESSENTIAL MED. EAGLE M0268 1983-09-12
K861867 Hazleton Research Products, Inc. MEM ALPHA EAGLE MEDIUM 1986-05-29
K821916 Dutchland Laboratories, Inc. IMPROVED MEM-RICHTER'S POWDER MODIF. 1982-07-27
K810767 Dutchland Laboratories, Inc. RPMI 1640 MEDIUM 1981-05-08

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004107906. Last updated year: 2026. Please use registration number 3004107906 when referencing this establishment in official correspondence.
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