LIFESTREAM PHARMA N.V.

FDA Device Registration & Listing · Seneffe Hainaut, BE · Registration 3012328521

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
3012328521
FEI Number
3012328521
Entity Name
LIFESTREAM PHARMA N.V.
City/State/Country
Seneffe Hainaut, BE
Establishment Address
Rue Jules Bordet, Zone C, Seneffe Hainaut 7180, BE
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device,Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device
Owner / Operator
OraBio, Inc. (Owner Number: 10089851)
Owner / Operator Contact Address
285 Kappa Drive, Suite 100, Pittsburgh, PA 15238, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K072306
PMA Number
N/A

All Registered Proprietary Names

PERIOVANCE BIOXTRA

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LFD Saliva, Artificial Unknown Class U N/A 2026-02-04

Official Correspondent

John Hauck

US Agent Details

John Hauck Business: OraBio, Inc. Email: john.hauck@orabio.com Phone: (724) 6005720

Related Public Records

Same Entity

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

Other Registrations for Same Entity

Registration Number Establishment Name Location
3030444281 ORABIO, INC. Pittsburgh, PA, US

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3012328521. Last updated year: 2026. Please use registration number 3012328521 when referencing this establishment in official correspondence.
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