Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3017189082

FEI Number

3017189082

Entity Name

MAVIDON MEDICAL PROD

City/State/Country

Flat Rock, NC, US

Establishment Address

110 Commercial Blvd, --, Flat Rock, NC 28731, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

MAVIDON MEDICAL PROD (Owner Number: 9036789)

Owner / Operator Contact Address

701 Oriole Dr, --, Hendersonville, NC 28792, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Medical Adhesive Remvoer Collodion Remover

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KOX	Solvent, Adhesive Tape	General, Plastic Surgery	Class 1	878.4730	2001-05-29

Official Correspondent

TIM CARROLL

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

MAVIDON MEDICAL PROD

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 3017189082. Last updated year: 2026. Please use registration number 3017189082 when referencing this establishment in official correspondence.