Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1044143

FEI Number

1000112898

Entity Name

PETER SCHIFF ENTERPRISE

City/State/Country

COOKEVILLE, TN, US

Establishment Address

4900 Forrest Hill Rd, COOKEVILLE, TN 38506, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

PETER SCHIFF ENTERPRISE (Owner Number: 1044143)

Owner / Operator Contact Address

4900 FORREST HILL RD., --, Cookeville, TN 38506, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

310C

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LIW	Fibrillator, Ac	Unknown	Class U	N/A	2010-03-09

Official Correspondent

Janice Scarlett

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

PETER SCHIFF ENTERPRISE

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 1044143. Last updated year: 2026. Please use registration number 1044143 when referencing this establishment in official correspondence.