LifeBot Inc

FDA Device Registration & Listing · Chicago, IL, US · Registration 3015194289

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
3015194289
FEI Number
3015194289
Entity Name
LifeBot Inc
City/State/Country
Chicago, IL, US
Establishment Address
1623 W Fulton St, Chicago, IL 60612, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
LifeBot Inc (Owner Number: 10042094)
Owner / Operator Contact Address
14 Oxford Road, New Rochelle, NY 10804, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

LifeBot 5 LifeBot Command DREAMS OS LifeBot Matrix DREAMS OS LifeBot 10 LifeBot Core DREAMS OS LifeBot 6 LifeBot Link DREAMS OS LifeBot 7 LifeBot Interceptor

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 2012-10-18

Official Correspondent

Jay Perl

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

LifeBot 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 3015194289. Last updated year: 2026. Please use registration number 3015194289 when referencing this establishment in official correspondence.
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