Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3002754225

FEI Number

3002754225

Entity Name

Emergency Products & Research, Inc.

City/State/Country

KENT, OH, US

Establishment Address

890 WEST MAIN STREET, KENT, OH 44240, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Emergency Products & Research, Inc. (Owner Number: 9060881)

Owner / Operator Contact Address

890 West Main Street, Kent, OH 44240, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Spider-Strap

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FPP	Stretcher, Hand-Carried	General Hospital	Class 1	880.6900	2004-01-30
FMQ	Restraint, Protective	General Hospital	Class 1	880.6760	2004-01-30
HSP	Splint, Traction	Orthopedic	Class 1	888.5890	2004-04-08
IQF	Orthosis, Cervical-Thoracic, Rigid	Physical Medicine	Class 1	890.3490	2004-01-30

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Emergency Products & Research, Inc.

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

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K962327	Sekure Seat Corp.	SEKURE SEAT ADULT PASSIVE RESTRAINING DEVICE	1997-03-06
K963243	Heelbo, Inc.	HEELBO BLAZER SLEEVED JACKET	1996-10-01

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3002754225. Last updated year: 2026. Please use registration number 3002754225 when referencing this establishment in official correspondence.