LIQUIDIA TECHNOLOGIES INC

FDA Device Registration & Listing · Morrisville, NC, US · Registration 3008731457

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
3008731457
FEI Number
3008731457
Entity Name
LIQUIDIA TECHNOLOGIES INC
City/State/Country
Morrisville, NC, US
Establishment Address
419 Davis Dr Ste 400, Morrisville, NC 27560, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198
Owner / Operator
Liquidia Technologies Inc (Owner Number: 10093826)
Owner / Operator Contact Address
419 Davis Dr #100, Morrisville, NC 27560, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Yutrepia

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KCJ Applicator, Ent Ear, Nose, Throat Class 1 874.5220 2025-07-17

Official Correspondent

Harold Alterson

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Liquidia Technologies Inc
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008731457. Last updated year: 2026. Please use registration number 3008731457 when referencing this establishment in official correspondence.
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