ORABIO, INC.

FDA Device Registration & Listing · Pittsburgh, PA, US · Registration 3030444281

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
3030444281
FEI Number
3030444281
Entity Name
ORABIO, INC.
City/State/Country
Pittsburgh, PA, US
Establishment Address
285 Kappa Dr Ste 100, Pittsburgh, PA 15238, US
Establishment Type(s)
Repack or Relabel 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
Y
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

No US Agent registered (Local establishment).

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
3012328521 LIFESTREAM PHARMA N.V. Seneffe Hainaut, BE

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3030444281. Last updated year: 2026. Please use registration number 3030444281 when referencing this establishment in official correspondence.
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