MRPC

FDA Device Registration & Listing · Butler, WI, US · Registration 3015239144

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3015239144
FEI Number
3015239144
Entity Name
MRPC
City/State/Country
Butler, WI, US
Establishment Address
13161 W. Glendale, Butler, WI 53007, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
MRPC (Owner Number: 10060167)
Owner / Operator Contact Address
13161 W. Glendale, Butler, WI 53007, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Smith and Nephew Finger Joint Bongo RX

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KYJ Prosthesis, Finger, Constrained, Polymer Orthopedic Class 2 888.3230 2024-02-06
OHP Expiratory Resistance Valve, Intranasal, For Obstructive Sleep Apnea Dental Class 2 872.5570 2019-04-05

Official Correspondent

Eric Powers

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

MRPC
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 3015239144. Last updated year: 2026. Please use registration number 3015239144 when referencing this establishment in official correspondence.
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