Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3005595687

FEI Number

3005595687

Entity Name

LEONHARDT MANUFACTURING CO, INC.

City/State/Country

Hanover, PA, US

Establishment Address

800 High Street, Hanover, PA 17331, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Leonhardt Manufacturing CO, Inc. (Owner Number: 10094202)

Owner / Operator Contact Address

800 High Street, Hanover, PA 17331, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
INF	Scale, Platform, Wheelchair	Physical Medicine	Class 1	890.3940	2025-11-18

Official Correspondent

Craig Aiello

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Leonhardt Manufacturing CO, Inc.

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

View Entity Profile →

Similar Registrations

Registration Number	Establishment Name	Location
3019300087	NAGATA SCALE CO., LTD.	Tainan City, TW
3032368	HOMECARE PRODUCTS, INC.	Auburn, WA, US
3003812504	CHARDER ELECTRONIC CO., LTD	Taichung City, TW
3011654863	SHENZHEN URION TECHNOLOGY CO., LTD.	Shenzhen Guangdong, CN
1821729	AMIGO MOBILITY INTL., INC.	BRIDGEPORT, MI, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005595687. Last updated year: 2026. Please use registration number 3005595687 when referencing this establishment in official correspondence.