ROGERS FOAM CORPORATION

FDA Device Registration & Listing · Mt Sterling, KY, US · Registration 3004082002

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
3004082002
FEI Number
3004082002
Entity Name
ROGERS FOAM CORPORATION
City/State/Country
Mt Sterling, KY, US
Establishment Address
310-A Flint Drive, Mt Sterling, KY 40353, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
ROGERS FOAM CORPORATION (Owner Number: 1216617)
Owner / Operator Contact Address
20 VERNON ST., --, Somerville, MA 02145, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Mattress Cover Foam Corner Protector

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IKY Mattress, Flotation Therapy, Non-Powered General Hospital Class 1 880.5150 2022-11-30
FMW Cover, Mattress (Medical Purposes) General Hospital Class 1 880.6190 2008-03-24
LRP Tray, Surgical General, Plastic Surgery Class 1 878.4800 2003-04-10

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

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

Other Registrations for Same Entity

Registration Number Establishment Name Location
3032847786 Cutters Foam Fabricating, Inc. Elkhart, IN, US
3015259843 Rogers Foam Corporation Morrisville, PA, US
3008314176 Rogers Foam Corporation Santa Teresa, NM, US
3009948565 Rogers Foam Juarez S de RL de CV Juarez Chihuahua, MX
3007307488 Rogers Foam Tijuana S. de R.L. de C.V. Tijuana Baja California, MX

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K881095 CooperVision, Inc. KOI(TM) INSTRUMENT TRAYS 1988-04-06

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0036-2010 Alphatec Spine, Inc. 1
ROC Lumbar bolt caddy, Part Number: 81997-01-05. Sterilization container for ROC bolts/screws. Product is used to contain spinal implants.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004082002. Last updated year: 2026. Please use registration number 3004082002 when referencing this establishment in official correspondence.
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