APNEICARE, LLC

FDA Device Registration & Listing · Columbus, OH, US · Registration 3007799743

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
3007799743
FEI Number
3007799743
Entity Name
APNEICARE, LLC
City/State/Country
Columbus, OH, US
Establishment Address
6185 Huntley Rd., Suite Q, Columbus, OH 43229, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device
Owner / Operator
ApneiCare, LLC (Owner Number: 10030013)
Owner / Operator Contact Address
6185 Huntley Rd., Suite Q, Columbus, OH 43229, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
K082968
PMA Number
N/A

All Registered Proprietary Names

SatCloud with Connection Center Patient Safety Connection Center Patient Safety SleepScreen Patient Safety SatScreen

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
OUG Medical Device Data System General Hospital Class 1 880.6310 2024-08-26
MNR Ventilatory Effort Recorder Anesthesiology Class 2 868.2375 2009-07-29

Official Correspondent

Craig Pickerill

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

ApneiCare, 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
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 3007799743. Last updated year: 2026. Please use registration number 3007799743 when referencing this establishment in official correspondence.
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