EXTHERA MEDICAL CORPORATION

FDA Device Registration & Listing · Martinez, CA, US · Registration 3014015528

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
3014015528
FEI Number
3014015528
Entity Name
EXTHERA MEDICAL CORPORATION
City/State/Country
Martinez, CA, US
Establishment Address
757 Arnold Drive, Suite B, Martinez, CA 94553, US
Establishment Type(s)
Manufacture Device in the United States for Export Only
Owner / Operator
ExThera Medical Corporation (Owner Number: 10075682)
Owner / Operator Contact Address
757 Arnold Drive, Suite B, Martinez, CA 94553, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Seraph 100 Microbind Affinity Blood Filter

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FLD Apparatus, Hemoperfusion, Sorbent Gastroenterology, Urology Class 2 876.5870 2020-06-23

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

ExThera Medical Corporation
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 3014015528. Last updated year: 2026. Please use registration number 3014015528 when referencing this establishment in official correspondence.
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