ATLAS LIFT TECH, INC.

FDA Device Registration & Listing · San Ramon, CA, US · Registration 3019594801

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
3019594801
FEI Number
3019594801
Entity Name
ATLAS LIFT TECH, INC.
City/State/Country
San Ramon, CA, US
Establishment Address
210 Porter Drive, Suite 300, San Ramon, CA 94583, US
Establishment Type(s)
Repack or Relabel Medical Device,Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Atlas Lift Tech (Owner Number: 10082183)
Owner / Operator Contact Address
210 Porter Drive, Suite 300, San Ramon, CA 94583, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Mobility monitor

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 2021-06-23

Official Correspondent

Richa Hussain

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Atlas Lift Tech
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 3019594801. Last updated year: 2026. Please use registration number 3019594801 when referencing this establishment in official correspondence.
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