LADY TECHNOLOGIES, INC.

FDA Device Registration & Listing · San Francisco, CA, US · Registration 3016725159

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
3016725159
FEI Number
3016725159
Entity Name
LADY TECHNOLOGIES, INC.
City/State/Country
San Francisco, CA, US
Establishment Address
2565 3rd St, Suite 318, South Building, San Francisco, CA 94107, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Lady Technologies, Inc. (Owner Number: 10066707)
Owner / Operator Contact Address
345 California St, Ste 600, San Francisco, CA 94104, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

kegg kegg

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KXQ Vibrator For Therapeutic Use, Genital Obstetrics/Gynecology Class 2 884.5960 2026-04-15
NGE Test, Luteinizing Hormone (Lh), Over The Counter Clinical Chemistry Class 1 862.1485 2020-04-02

Official Correspondent

Kristina Cahojova

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Lady Technologies, Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0043-2024 Universal Meditech Inc. 1
One Step Ovulation Test REF 200-01

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3016725159. Last updated year: 2026. Please use registration number 3016725159 when referencing this establishment in official correspondence.
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