GEMINI BIOPRODUCTS LLC

FDA Device Registration & Listing · West Sacramento, CA, US · Registration 3006236690

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
3006236690
FEI Number
3006236690
Entity Name
GEMINI BIOPRODUCTS LLC
City/State/Country
West Sacramento, CA, US
Establishment Address
920 Stillwater Road, Suite 130, West Sacramento, CA 95605, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device
Owner / Operator
Gemini Bioproducts LLC (Owner Number: 10058502)
Owner / Operator Contact Address
920 Stillwater Road, Suite 130, West Sacramento, CA 95605, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

GemCell GemCell GemCell

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KIS Sera, Animal And Human Hematology Class 1 864.2800 2018-10-05
KIT Media And Components, Synthetic Cell And Tissue Culture Hematology Class 1 864.2220 2020-06-02
KIP Formulations, Balanced Salt Solutions Hematology Class 1 864.2875 2020-06-02

Official Correspondent

Rob Perry

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Gemini Bioproducts 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 3006236690. Last updated year: 2026. Please use registration number 3006236690 when referencing this establishment in official correspondence.
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