EXPRESSION SYSTEMS LLC.

FDA Device Registration & Listing · Davis, CA, US · Registration 3005875593

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
3005875593
FEI Number
3005875593
Entity Name
EXPRESSION SYSTEMS LLC.
City/State/Country
Davis, CA, US
Establishment Address
2537 2nd St, Davis, CA 95618, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
EXPRESSION SYSTEMS LLC. (Owner Number: 9090779)
Owner / Operator Contact Address
2537 2nd Street, Davis, CA 95618, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

; ESF 921 Insect Cell Culture Medium, Protein Free Baculovirus Titering Kit ESF AF Insect Cell Culture Medium, Animal Free ESF SFM Mammalian Cell Culture Medium, Serum Free Medium gp64-PE Antibody; PBA—Production BoostAdditive

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KIT Media And Components, Synthetic Cell And Tissue Culture Hematology Class 1 864.2220 2006-08-07

Official Correspondent

Philip Cole IV

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

EXPRESSION SYSTEMS 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 3005875593. Last updated year: 2026. Please use registration number 3005875593 when referencing this establishment in official correspondence.
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