DEEPHEALTH

FDA Device Registration & Listing · Somerville, MA, US · Registration 3018733944

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
3018733944
FEI Number
3018733944
Entity Name
DEEPHEALTH
City/State/Country
Somerville, MA, US
Establishment Address
212 Elm St., Somerville, MA 02144, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
DeepHealth (Owner Number: 10081546)
Owner / Operator Contact Address
212 Elm St., Somerville, MA 02144, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

TechLive Saige-Dx Saige-Density SmartMammo Density Saige-Q SmartMammoDx Saige-Dx ThinQ Brain Age Saige-Assure

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LLZ System, Image Processing, Radiological Radiology Class 2 892.2050 2025-11-18
QDQ Radiological Computer Assisted Detection/Diagnosis Software For Lesions Suspicious For Cancer Radiology Class 2 892.2090 2025-11-18
QIH Automated Radiological Image Processing Software Radiology Class 2 892.2050 2022-12-29
QFM Radiological Computer-Assisted Prioritization Software For Lesions Radiology Class 2 892.2080 2021-04-22
QDQ Radiological Computer Assisted Detection/Diagnosis Software For Lesions Suspicious For Cancer Radiology Class 2 892.2090 2024-11-26
LLZ System, Image Processing, Radiological Radiology Class 2 892.2050 2025-11-18
LMD System, Digital Image Communications, Radiological Radiology Class 1 892.2020 2023-09-07

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

DeepHealth
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K080013 Agfa Healthcare Corporation REGISTRATION AND FUSION 2008-01-17
K042221 Barco NV Barcoview CORONIS 5MP MEDICAL FLAT PANEL DISPLAY SYSTEM 2004-12-30
K092915 Cedara Software Corp. CEDARA WEBACCESS, MODEL: 2.4 2010-06-23
K961871 Siemens Medical Solutions USA, Inc. FLOUROSPOT T.O.P. 1996-07-31
K122260 Aycan Digitalsysteme GmbH AYCAN MOBILE 2012-09-12

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0012-2022 GE Healthcare, LLC 2
Centricity Universal Viewer 7.0, Model 5829628-0XX. Radiological image processing system
Z-0023-2016 GE Healthcare 2
Centricity PACS IW by GE Healthcare Dynamic Imaging Solutions is a device that receives medical images (including mammograms) and data from various imaging sources. Images and data can be stored, communicated, processed and displayed within the system or across computer networks at distributed locations.
Z-0030-2026 CHANGE HEALTHCARE CANADA COMPANY 2
Change Healthcare Radiology Solutions software version 14.2.2
Z-0032-2012 Philips Healthcare Inc. 2
MDC PACS - release R2.3 SP1 . Phillips Healthcare Andover, Massachusetts A software application that is used for receiving, managing, archiving, distributing and recording medical images onto portable digital media (including but not limited to Compact Disk and DVD).
Z-0033-2007 AGFA Corp. 2
IMPAX 5.2 Systems with CAD Capability (Computer Assisted Diagnosis)

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3018733944. Last updated year: 2026. Please use registration number 3018733944 when referencing this establishment in official correspondence.
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