Halo Dream, Inc.

FDA Device Registration & Listing · New York, NY, US · Registration 3006606837

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
3006606837
FEI Number
3006606837
Entity Name
Halo Dream, Inc.
City/State/Country
New York, NY, US
Establishment Address
213 West 35th Street, Suite 12W, New York, NY 10001, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Halo Dream, Inc. (Owner Number: 10052419)
Owner / Operator Contact Address
213 West 35th Street, Suite 12W, New York, NY 10001, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

HALO Bassinest Hospital Series HALO Hospital Bassinest Swivel Sleeper

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NZG Bassinet, Hospital General Hospital Class 2 880.5145 2018-12-13

Official Correspondent

Thomas Crimmins

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Halo Dream, Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3006606837. Last updated year: 2026. Please use registration number 3006606837 when referencing this establishment in official correspondence.
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