Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3041913476

FEI Number

3041913476

Entity Name

AVANT-GARDE MEDICAL INNOVATION

City/State/Country

Ponte Vedra Beach, FL, US

Establishment Address

124 Montura Dr, Ponte Vedra Beach, FL 32082, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

Avant-Garde Medical Innovation (Owner Number: 10094365)

Owner / Operator Contact Address

124 Montura Dr, Ponte Vedra Beach, FL 32082, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

MIDAS Chest Tube Dressing

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NAE	Dressing, Wound, Hydrogel Without Drug And/Or Biologic	General, Plastic Surgery	Class 1	878.4022	2025-11-25

Official Correspondent

Julia Wilke

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Avant-Garde Medical Innovation

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 3041913476. Last updated year: 2026. Please use registration number 3041913476 when referencing this establishment in official correspondence.