CONSOLIDATED RESEARCH, INC.

FDA Device Registration & Listing · Euclid, OH, US · Registration 3009770872

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
3009770872
FEI Number
3009770872
Entity Name
CONSOLIDATED RESEARCH, INC.
City/State/Country
Euclid, OH, US
Establishment Address
26250 Euclid Ave Ste 709, Euclid, OH 44132, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Consolidated Research, Inc. (Owner Number: 10041808)
Owner / Operator Contact Address
26250 Euclid Ave., Suite 709, Euclid, OH 44132, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K172986
PMA Number
N/A

All Registered Proprietary Names

Zmachine DT-100 Zmachine Synergy Zmachine DT-300

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
OLV Standard Polysomnograph With Electroencephalograph Neurology Class 2 882.1400 2012-09-05
OMC Reduced- Montage Standard Electroencephalograph Neurology Class 2 882.1400 2012-09-05
OLV Standard Polysomnograph With Electroencephalograph Neurology Class 2 882.1400 2017-12-24
OMC Reduced- Montage Standard Electroencephalograph Neurology Class 2 882.1400 2017-12-24
MNR Ventilatory Effort Recorder Anesthesiology Class 2 868.2375 2017-12-24

Official Correspondent

Richard Kaplan

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Consolidated Research, 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
K161650 Neurotronics, Inc. Polysmith Sleep System, Model NTI7593 2017-01-19
K082968 Apneicare, LLC APNEICARE CONNECTION CENTER/INTERNET ANALYSIS 2009-01-02

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0031-2022 NOX MEDICAL Keldnaholt Reykjavik Iceland 2
Nox T3s Recorder - Product Usage: intended for ambulatory recording of physiological signals during sleep.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009770872. Last updated year: 2026. Please use registration number 3009770872 when referencing this establishment in official correspondence.
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