SLEEP GROUP SOLUTIONS

FDA Device Registration & Listing · Hollywood, FL, US · Registration 3007075845

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
3007075845
FEI Number
3007075845
Entity Name
SLEEP GROUP SOLUTIONS
City/State/Country
Hollywood, FL, US
Establishment Address
2035 Harding St Ste 200, Hollywood, FL 33020, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Sleep Group Solutions (Owner Number: 10024742)
Owner / Operator Contact Address
2035 Harding Street, Ste #200, Hollywood, FL 33020, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K170071
PMA Number
N/A

All Registered Proprietary Names

SGS Eccovision Rhinometer ECCOVISION

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
BXQ Rhinoanemometer (Measurement Of Nasal Decongestion) Anesthesiology Class 2 868.1800 2008-02-20
BXQ Rhinoanemometer (Measurement Of Nasal Decongestion) Anesthesiology Class 2 868.1800 2018-03-19

Official Correspondent

Rani Ben-David

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Sleep Group Solutions
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 3007075845. Last updated year: 2026. Please use registration number 3007075845 when referencing this establishment in official correspondence.
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