Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

2531191

FEI Number

3000207346

Entity Name

J.P. GILBERT CO.

City/State/Country

BOYERTOWN, PA, US

Establishment Address

548 Mountain Rd, BOYERTOWN, PA 19512, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

J.P. GILBERT CO. (Owner Number: 9027898)

Owner / Operator Contact Address

548 MOUNTAIN RD., --, Gabelsville, PA 19512, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

MINIPREP

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
GKJ	Spinner, Slide, Automated	Hematology	Class 1	864.5850	1996-09-19

Official Correspondent

CHARLES GILBERT

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

J.P. GILBERT CO.

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 2531191. Last updated year: 2026. Please use registration number 2531191 when referencing this establishment in official correspondence.