Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3019248313

FEI Number

3019248313

Entity Name

REALIZED MFG

City/State/Country

Medina, OH, US

Establishment Address

879 S. Progress Drive, Suite A, Medina, OH 44256, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Realized Mfg. (Owner Number: 10084896)

Owner / Operator Contact Address

879 S. Progress Drive, Suite A, Medina, OH 44256, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
PBF	Orthopaedic Surgical Planning And Instrument Guides	Orthopedic	Class 2	888.3030	2025-03-18

Official Correspondent

Michael Rappach

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Realized Mfg.

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 3019248313. Last updated year: 2026. Please use registration number 3019248313 when referencing this establishment in official correspondence.