AEM CORP.

FDA Device Registration & Listing · Renton, WA, US · Registration 3009523656

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
3009523656
FEI Number
3009523656
Entity Name
AEM CORP.
City/State/Country
Renton, WA, US
Establishment Address
11602 SE 163rd St, Renton, WA 98058, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
AEM Corp. (Owner Number: 10040333)
Owner / Operator Contact Address
11602 SE 163rd St, Renton, WA 98058, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Birth Pool in a Box Edel Immersys FP3

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
OVX Water Immersion Labor Pool Unknown Class N N/A 2017-04-13

Official Correspondent

Adam Maclean

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

AEM Corp.
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 3009523656. Last updated year: 2026. Please use registration number 3009523656 when referencing this establishment in official correspondence.
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