Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3006892202

FEI Number

3006892202

Entity Name

PHYTOGENX, INC.

City/State/Country

Morgantown, PA, US

Establishment Address

35 Thousand Oaks Blvd, Morgantown, PA 19543, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

PhytogenX, Inc. (Owner Number: 10050936)

Owner / Operator Contact Address

35 Thousand Oaks Blvd, Morgantown, PA 19543, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Satisfaite

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NUC	Lubricant, Personal	Obstetrics/Gynecology	Class 2	884.5300	2020-02-24

Official Correspondent

Julie Panzner

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

PhytogenX, Inc.

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 3006892202. Last updated year: 2026. Please use registration number 3006892202 when referencing this establishment in official correspondence.