Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3015544237

FEI Number

3015544237

Entity Name

WISCMED, LLC

City/State/Country

Middleton, WI, US

Establishment Address

8383 Greenway Blvd, Suite 600, Middleton, WI 53562, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

WiscMed, LLC (Owner Number: 10060383)

Owner / Operator Contact Address

8383 Greenway Blvd, Suite 600, Middleton, WI 53562, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

WiscMed Wispr

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
ERA	Otoscope	Ear, Nose, Throat	Class 1	874.4770	2019-05-05

Official Correspondent

James Berbee

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

WiscMed, LLC

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

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K932506	Rudolf Riester GmbH & Co. KG	RI-SCOPE (S)	1993-10-08

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015544237. Last updated year: 2026. Please use registration number 3015544237 when referencing this establishment in official correspondence.