GRUMPY INNOVATION INC

FDA Device Registration & Listing · Sioux Falls, SD, US · Registration 3044675089

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
3044675089
FEI Number
3044675089
Entity Name
GRUMPY INNOVATION INC
City/State/Country
Sioux Falls, SD, US
Establishment Address
100 E 6th St, Sioux Falls, SD 57104, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Grumpy Innovation Inc (Owner Number: 10095709)
Owner / Operator Contact Address
2601 S Minnesota Ave, Ste 105, Sioux Falls, SD 57105, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Portare System

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EOB Nasopharyngoscope (Flexible Or Rigid) Ear, Nose, Throat Class 2 874.4760 2026-04-16

Official Correspondent

Tiffni Wittwer

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Grumpy Innovation Inc
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3044675089. Last updated year: 2026. Please use registration number 3044675089 when referencing this establishment in official correspondence.
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