CEEK WOMEN'S HEALTH

FDA Device Registration & Listing · Portland, OR, US · Registration 3014902417

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
3014902417
FEI Number
3014902417
Entity Name
CEEK WOMEN'S HEALTH
City/State/Country
Portland, OR, US
Establishment Address
2175 NW Raleigh Street, Suite 110, Portland, OR 97210, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Ceek Women's Health (Owner Number: 10058318)
Owner / Operator Contact Address
2175 NW Raleigh Street, Suite 110, Portland, OR 97210, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

VuLight Nella Comfort Kit Maternity Nella Next Single Use Nella Comfort Kit Curves Nella Comfort Kit Menopause Nella Single Use Nella Reusable Nella Comfort Kit FirstTime Nella Comfort Kit Classic

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KYT Light, Examination, Medical, Battery Powered General Hospital Class 1 880.6350 2020-03-12
HIB Speculum, Vaginal, Nonmetal Obstetrics/Gynecology Class 2 884.4530 2020-01-30

Official Correspondent

Tracy Bennett

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Ceek Women's Health
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 3014902417. Last updated year: 2026. Please use registration number 3014902417 when referencing this establishment in official correspondence.
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