ALTAMONT SOFTWARE, INC.

FDA Device Registration & Listing · Pleasanton, CA, US · Registration 3018069403

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
3018069403
FEI Number
3018069403
Entity Name
ALTAMONT SOFTWARE, INC.
City/State/Country
Pleasanton, CA, US
Establishment Address
127 Spring Street, Suite 110, Pleasanton, CA 94566, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Altamont Software, Inc. (Owner Number: 10080739)
Owner / Operator Contact Address
127 Spring Street, Suite 110, Pleasanton, CA 94566, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Altamont CaptureWare Altamont Passport Altamont Outbox

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LMD System, Digital Image Communications, Radiological Radiology Class 1 892.2020 2021-02-23

Official Correspondent

Brian Cavanaugh

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Altamont Software, 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 3018069403. Last updated year: 2026. Please use registration number 3018069403 when referencing this establishment in official correspondence.
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