ILION MEDICAL INC

FDA Device Registration & Listing · Minneapolis, MN, US · Registration 3014919610

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
3014919610
FEI Number
3014919610
Entity Name
ILION MEDICAL INC
City/State/Country
Minneapolis, MN, US
Establishment Address
Medical Arts Building, 825 Nicollet Mall, Suite 700, Minneapolis, MN 55402, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Ilion Medical Inc (Owner Number: 10088627)
Owner / Operator Contact Address
Medical Arts Building, 825 Nicollet Mall, Suite 700, Minneapolis, MN 55402, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

NADIA Sacroiliac Fusion Implant

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
OUR Sacroiliac Joint Fixation Orthopedic Class 2 888.3040 2023-09-07

Official Correspondent

Tania Fuentes-Davitt

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Ilion Medical 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
K213667 SI-BONE, Inc. iFuse-TORQ® Implant System 2022-06-10

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014919610. Last updated year: 2026. Please use registration number 3014919610 when referencing this establishment in official correspondence.
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