MD LABS, LLC

FDA Device Registration & Listing · Westlake Village, CA, US · Registration 3027686087

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
3027686087
FEI Number
3027686087
Entity Name
MD LABS, LLC
City/State/Country
Westlake Village, CA, US
Establishment Address
780 Lakefield Rd., Unit H, Westlake Village, CA 91361, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
MD Labs, LLC (Owner Number: 10087273)
Owner / Operator Contact Address
780 Lakefield Rd., Unit H, Westlake Village, CA 91361, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K230518
PMA Number
N/A

All Registered Proprietary Names

HydraDose Vaginal Suppositories VLUSH BEAUTY Vaginal Moisturizer Suppositories

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NUC Lubricant, Personal Obstetrics/Gynecology Class 2 884.5300 2023-08-02

Official Correspondent

Harout Achekian

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

MD Labs, 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
K050212 Qualis, Inc. PERSONAL WARMING JELLY 2005-03-17

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3027686087. Last updated year: 2026. Please use registration number 3027686087 when referencing this establishment in official correspondence.
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