Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3004612223

FEI Number

3004612223

Entity Name

Aprios Custom Mfg.

City/State/Country

Minneapolis, MN, US

Establishment Address

8617 Xylon Ct, Minneapolis, MN 55445, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Diversified Plastics, Inc (Owner Number: 10043677)

Owner / Operator Contact Address

8617 Xylon Court North, Minneapolis, MN 55445, 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
JRL	Unit, Filter, Membrane	Clinical Chemistry	Class 1	862.2050	2024-02-06
OTN	Mesh, Surgical, Synthetic, Urogynecologic, For Stress Urinary Incontinence, Retropubic Or Transobturator	General, Plastic Surgery	Class 2	878.3300	2026-04-25
PAH	Mesh, Surgical, Synthetic, Urogynecologic, For Stress Urinary Incontinence, Female, Mini-Sling	General, Plastic Surgery	Class 2	878.3300	2026-04-25

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Diversified Plastics, Inc

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K812750	Instrumentation Laboratory CO	IL 703, STAT SEPARATOR	1982-01-26
K222293	Urocure, LLC	ArcSP Suprapubic Sling System	2022-09-21

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1721504	MERIT MEDICAL SYSTEMS, INC.	South Jordan, UT, US
3009893608	AQUAMEDIX	Eden Prairie, MN, US
3033589330	Merit Medical Australia Pty Ltd.	Braiside Victoria, AU

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004612223. Last updated year: 2026. Please use registration number 3004612223 when referencing this establishment in official correspondence.