FOAMCRAFT, INC.

FDA Device Registration & Listing · Greenfield, IN, US · Registration 3008879671

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
3008879671
FEI Number
3008879671
Entity Name
FOAMCRAFT, INC.
City/State/Country
Greenfield, IN, US
Establishment Address
7213 W 200 N, Greenfield, IN 46140, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Foamcraft, Inc. (Owner Number: 10032948)
Owner / Operator Contact Address
7213 W 200 N, Greenfield, IN 46140, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Skin Pressure Protector Patient Support Position

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FMP Protector, Skin Pressure General Hospital Class 1 880.6450 2010-06-28
CCX Support, Patient Position Anesthesiology Class 1 868.6820 2010-06-28

Official Correspondent

Joe Elliott

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Foamcraft, 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 3008879671. Last updated year: 2026. Please use registration number 3008879671 when referencing this establishment in official correspondence.
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