K-FIT KEGEL TONER, LLC

FDA Device Registration & Listing · Albany, OR, US · Registration 3014405438

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
3014405438
FEI Number
3014405438
Entity Name
K-FIT KEGEL TONER, LLC
City/State/Country
Albany, OR, US
Establishment Address
2373 Cluster Oak Ave NW, Albany, OR 97321, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198
Owner / Operator
K-fit Kegel Toner, LLC (Owner Number: 10057321)
Owner / Operator Contact Address
2373 Cluster Oak Ave NW, Albany, OR 97321, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

K-fit Kegel Toner KM518

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KPI Stimulator, Electrical, Non-Implantable, For Incontinence Gastroenterology, Urology Class 2 876.5320 2026-03-24

Official Correspondent

Aimee Roseland

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

K-fit Kegel Toner, LLC
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 3014405438. Last updated year: 2026. Please use registration number 3014405438 when referencing this establishment in official correspondence.
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