Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3015909322

FEI Number

1000526105

Entity Name

EDM 3, LLC

City/State/Country

Jacksonville, FL, US

Establishment Address

3611 St Johns Bluff Rd S #1, Jacksonville, FL 32224, US

Establishment Type(s)

Repack or Relabel Medical Device,Manufacture Medical Device

Owner / Operator

EDM 3, LLC (Owner Number: 10061440)

Owner / Operator Contact Address

3611 St Johns Bluff Rd S #1, Jacksonville, FL 32224, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K921822

PMA Number

N/A

All Registered Proprietary Names

EDM3 Biopsy Punch

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MDM	Instrument, Manual, Surgical, General Use	General, Plastic Surgery	Class 1	878.4800	2019-10-18

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

EDM 3, LLC

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 3015909322. Last updated year: 2026. Please use registration number 3015909322 when referencing this establishment in official correspondence.