HemaTerra Technologies, LLC

FDA Device Registration & Listing · Baltimore, MD, US · Registration 3015108978

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
3015108978
FEI Number
3015108978
Entity Name
HemaTerra Technologies, LLC
City/State/Country
Baltimore, MD, US
Establishment Address
180 West Ostend Street, Suite 267A, Baltimore, MD 21230, US
Establishment Type(s)
Manufacture Medical Device,Complaint File Establishment per 21 CFR 820.198
Owner / Operator
HemaTerra Technologies, LLC (Owner Number: 10086581)
Owner / Operator Contact Address
180 West Ostend Street, Suite 267A, Baltimore, MD 21230, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
BK210620
PMA Number
N/A

All Registered Proprietary Names

BloodRelay version 1.1 and later

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MMH Blood Establishment Computer Software And Accessories Hematology Class 2 864.9165 2022-11-21

Official Correspondent

Debra Vigil

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

HemaTerra Technologies, LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015108978. Last updated year: 2026. Please use registration number 3015108978 when referencing this establishment in official correspondence.
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