Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1000227151

FEI Number

1000227151

Entity Name

RAULAND-BORG CORPORATION

City/State/Country

Mount Prospect, IL, US

Establishment Address

1802 West Central Road, Mount Prospect, IL 60056, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Rauland (Ametek) (Owner Number: 9075142)

Owner / Operator Contact Address

1802 West Central Road, --, Mount Prospect, IL 60056, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Responder

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
OUG	Medical Device Data System	General Hospital	Class 1	880.6310	2017-11-20

Official Correspondent

Peter Sparacio

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Rauland (Ametek)

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

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
3025306510	AMETEK LAMB MOTORES DE MEXICO S. DE R.L. DE C.V.	Nuevo Laredo Tamaulipas, MX

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1000227151. Last updated year: 2026. Please use registration number 1000227151 when referencing this establishment in official correspondence.