Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3013727038

FEI Number

3013727038

Entity Name

am foam products

City/State/Country

Kansas City, MO, US

Establishment Address

3255 east 18th, Kansas City, MO 64127, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

strako enterprises (Owner Number: 10055259)

Owner / Operator Contact Address

3255 east 18th, Kansas City, MO 64127, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KIA	Cover, Cast	General Hospital	Class 1	880.6185	2017-06-27

Official Correspondent

joe ebeck

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

strako enterprises

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Similar Registrations

Registration Number	Establishment Name	Location
3019312260	MCADAM LLOYD INC	Chicago, IL, US
3013876064	PRECISION DIPPING MANUFACTURING LTD	Yate Bristol, City of, GB
3014847663	ASIA QUALITY & TECHNICAL SERVICES INC. (ASIA TECHNICAL SERVICES)	Taichung City, TW
2182318	TIDI PRODUCTS, LLC	NEENAH, WI, US
1926174	Brownmed	Spirit Lake, IA, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013727038. Last updated year: 2026. Please use registration number 3013727038 when referencing this establishment in official correspondence.