SENTINEL MEDICAL TECHNOLOGIES, LLC

FDA Device Registration & Listing · Jacksonville, FL, US · Registration 3021468326

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
3021468326
FEI Number
3021468326
Entity Name
SENTINEL MEDICAL TECHNOLOGIES, LLC
City/State/Country
Jacksonville, FL, US
Establishment Address
50 N Laura St Ste 2500, Jacksonville, FL 32202, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Sentinel Medical Technologies, LLC (Owner Number: 10083817)
Owner / Operator Contact Address
50 N Laura Dr, Suite 2500, Jacksonville, FL 32202, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

TraumaGuard Intra-abdominal Pressure Monitoring System

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
PHU Intra-Abdominal Pressure Monitoring Device Unknown Class U N/A 2021-12-21

Official Correspondent

Jackelyn Rodriguez

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Sentinel Medical 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 3021468326. Last updated year: 2026. Please use registration number 3021468326 when referencing this establishment in official correspondence.
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