ALEVIO, LLC

FDA Device Registration & Listing · Cullman, AL, US · Registration 3012249461

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
3012249461
FEI Number
3012249461
Entity Name
ALEVIO, LLC
City/State/Country
Cullman, AL, US
Establishment Address
17721 Us Highway 31, Cullman, AL 35058, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
ALEVIO, LLC (Owner Number: 10051119)
Owner / Operator Contact Address
200 CAHABA PARK CIRCLE, SUITE 100, Birmingham, AL 35242, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K223819
PMA Number
N/A

All Registered Proprietary Names

SI-CURE: FOUNDATION, SACROILIAC JOINT FUSION SYSTEM SI-CURE SACROILIAC JOINT FUSION SYSTEM SI-CURE: MICRO, SACROILIAC JOINT FUSION SYSTEM

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
OUR Sacroiliac Joint Fixation Orthopedic Class 2 888.3040 2025-02-25

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

ALEVIO, LLC
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 3012249461. Last updated year: 2026. Please use registration number 3012249461 when referencing this establishment in official correspondence.
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