Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

2531348

FEI Number

3001238948

Entity Name

C. L. STURKEY, INC.

City/State/Country

Lebanon, PA, US

Establishment Address

824 Cumberland Street, Lebanon, PA 17042, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

C. L. Sturkey, Inc. (Owner Number: 10025927)

Owner / Operator Contact Address

824 Cumberland Street, Lebanon, PA 17042, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Sturkey

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
IDL	Microtome, Accessories	Pathology	Class 1	864.3010	2008-05-21

Official Correspondent

Christopher Tarsa

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

C. L. Sturkey, Inc.

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 2531348. Last updated year: 2026. Please use registration number 2531348 when referencing this establishment in official correspondence.