BAHIA MEDICAL

FDA Device Registration & Listing · Plano, TX, US · Registration 3044620161

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
3044620161
FEI Number
3044620161
Entity Name
BAHIA MEDICAL
City/State/Country
Plano, TX, US
Establishment Address
7250 Dallas Pkwy Ste 400, Plano, TX 75024, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Bahia Medical (Owner Number: 10095503)
Owner / Operator Contact Address
4 Autry, Irvine, CA 92618, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
BK251248
PMA Number
N/A

All Registered Proprietary Names

Margenix PRP

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ORG Platelet And Plasma Separator For Bone Graft Handling Hematology Class 2 864.9245 2026-03-20

Official Correspondent

Luis Mendoza

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Bahia Medical
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 3044620161. Last updated year: 2026. Please use registration number 3044620161 when referencing this establishment in official correspondence.
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