Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3031001105

FEI Number

3031001105

Entity Name

SOLABORATE INC.

City/State/Country

Clearwater, FL, US

Establishment Address

2605 Enterprise RD E Suite 150, Clearwater, FL 33759, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Solaborate Inc. (Owner Number: 10089469)

Owner / Operator Contact Address

2605 Enterprise RD E Suite 150, Clearwater, FL 33759, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

hellocare HELLO

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KMI	Monitor, Bed Patient	General Hospital	Class 1	880.2400	2024-04-04

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Solaborate Inc.

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 3031001105. Last updated year: 2026. Please use registration number 3031001105 when referencing this establishment in official correspondence.