DEEP BLUE MEDICAL ADVANCES, INC.

FDA Device Registration & Listing · Durham, NC, US · Registration 3017492634

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
3017492634
FEI Number
3017492634
Entity Name
DEEP BLUE MEDICAL ADVANCES, INC.
City/State/Country
Durham, NC, US
Establishment Address
701 W Main Street, Suite 410, Durham, NC 27701, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Deep Blue Medical Advances, Inc. (Owner Number: 10078119)
Owner / Operator Contact Address
701 W Main St #410, Durham, NC 27701, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K193144
PMA Number
N/A

All Registered Proprietary Names

T-Line Hernia Mesh

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FTL Mesh, Surgical, Polymeric General, Plastic Surgery Class 2 878.3300 2020-10-11

Official Correspondent

Lou Fuqua

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Deep Blue Medical Advances, Inc.
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
K220540 Covidien ProGrip Self-Gripping Polypropylene Mesh 2022-09-22

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3017492634. Last updated year: 2026. Please use registration number 3017492634 when referencing this establishment in official correspondence.
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