Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3029779

FEI Number

1000523895

Entity Name

DAVRYAN LABORATORIES, INC.

City/State/Country

Valparaiso, IN, US

Establishment Address

844 Mirmar Dr, Valparaiso, IN 46385, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

DAVRYAN LABORATORIES, INC. (Owner Number: 9012184)

Owner / Operator Contact Address

844 Mirmar Dr, --, Valparaiso, IN 46385, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K952465

PMA Number

N/A

All Registered Proprietary Names

Probe Personal Lubricant Thick Rich Probe Personal Lubricant Silky Light

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HIS	Condom	Obstetrics/Gynecology	Class 2	884.5300	2007-10-30
HIS	Condom	Obstetrics/Gynecology	Class 2	884.5300	2007-11-01

Official Correspondent

Kenneth Bruster

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

DAVRYAN LABORATORIES, INC.

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 3029779. Last updated year: 2026. Please use registration number 3029779 when referencing this establishment in official correspondence.