APOSTLE INC.

FDA Device Registration & Listing · Pleasanton, CA, US · Registration 3017583200

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
3017583200
FEI Number
3017583200
Entity Name
APOSTLE INC.
City/State/Country
Pleasanton, CA, US
Establishment Address
3589 Nevada Street, Pleasanton, CA 94566, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Apostle Inc. (Owner Number: 10087051)
Owner / Operator Contact Address
3589 Nevada Street, Pleasanton, CA 94566, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

CheckMeSafe Urine Collection Kit MiniMax® High Efficiency Cell-Free DNA Isolation Kit

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
OIE Urine Collection Kit (Excludes Hiv Testing) Pathology Class 1 864.3250 2023-01-05
JJH Clinical Sample Concentrator Clinical Chemistry Class 1 862.2310 2026-03-02

Official Correspondent

Yi Shen

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Apostle Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3017583200. Last updated year: 2026. Please use registration number 3017583200 when referencing this establishment in official correspondence.
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