3DPX MEDICAL

FDA Device Registration & Listing · Chicago, IL, US · Registration 3017567754

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3017567754
FEI Number
3017567754
Entity Name
3DPX MEDICAL
City/State/Country
Chicago, IL, US
Establishment Address
410 N Milwaukee Ave Suite 100, Chicago, IL 60607, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
3DPX Medical (Owner Number: 10078770)
Owner / Operator Contact Address
410 N Milwaukee Ave Suite 100, Chicago, IL 60654, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Night Guard

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LRK Device, Anti-Snoring Dental Class 2 872.5570 2021-03-11
OCO Mouthguard, Migraine/Tension Headache Unknown Class U N/A 2025-02-27
MQC Mouthguard, Prescription Unknown Class U N/A 2025-02-27

Official Correspondent

Sarah Moss

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

3DPX Medical
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
K122391 Medtronic Xomed, Inc. MEDTRONIC XOMED, INC. 2013-01-10

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3017567754. Last updated year: 2026. Please use registration number 3017567754 when referencing this establishment in official correspondence.
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