AUTOMATEDASSESSMENTS

FDA Device Registration & Listing · Omaha, NE, US · Registration 3031840757

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
3031840757
FEI Number
3031840757
Entity Name
AUTOMATEDASSESSMENTS
City/State/Country
Omaha, NE, US
Establishment Address
3323 N 161st Ter, Omaha, NE 68116, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
AutomatedAssessments (Owner Number: 10091153)
Owner / Operator Contact Address
3323 N 161st Terrace, Omaha, NE 68116, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

VITAL-IT

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HRW Dynamometer, Nonpowered Orthopedic Class 1 888.1250 2024-07-13

Official Correspondent

Jason Johanning

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

AutomatedAssessments
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3031840757. Last updated year: 2026. Please use registration number 3031840757 when referencing this establishment in official correspondence.
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