AOA PRODUCTS LLC

FDA Device Registration & Listing · Toledo, OH, US · Registration 3007630531

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
3007630531
FEI Number
3007630531
Entity Name
AOA PRODUCTS LLC
City/State/Country
Toledo, OH, US
Establishment Address
3618 KING RD., UNIT D, Toledo, OH 43617, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
AOA PRODUCTS LLC (Owner Number: 10095135)
Owner / Operator Contact Address
3618 KING RD., UNIT D, Toledo, OH 43617, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K222428
PMA Number
N/A

All Registered Proprietary Names

syngo Dymamics

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
QIH Automated Radiological Image Processing Software Radiology Class 2 892.2050 2026-01-27

Official Correspondent

ALMA ALBRIGHT

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

AOA PRODUCTS 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
K242270 Orthofix Srl OrthoNext Platform System 2024-12-19
K261713 FUJIFILM Healthcare Americas Corporation Synapse PACS (7.6.0) 2026-06-18
K243647 FUJIFILM Healthcare Americas Corporation Synapse PACS (7.5) 2025-06-30

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007630531. Last updated year: 2026. Please use registration number 3007630531 when referencing this establishment in official correspondence.
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