ALIFE HEALTH, INC.

FDA Device Registration & Listing · San Francisco, CA, US · Registration 3042372505

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
3042372505
FEI Number
3042372505
Entity Name
ALIFE HEALTH, INC.
City/State/Country
San Francisco, CA, US
Establishment Address
3717 Buchanan St, San Francisco, CA 94123, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Alife Health, Inc. (Owner Number: 10094304)
Owner / Operator Contact Address
3717 Buchanan St, San Francisco, CA 94123, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K250781
PMA Number
N/A

All Registered Proprietary Names

Embryo Predict

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
PBH Embryo Image Assessment System, Assisted Reproduction Obstetrics/Gynecology Class 2 884.6195 2026-05-22

Official Correspondent

Grace Bartoo

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Alife Health, 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 3042372505. Last updated year: 2026. Please use registration number 3042372505 when referencing this establishment in official correspondence.
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