Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3007935577

FEI Number

3007935577

Entity Name

UNITHER LIQUID MANUFACTURING

City/State/Country

COLOMIERS Haute-Garonne, FR

Establishment Address

1,3 allee de la neste, COLOMIERS Haute-Garonne 31770, FR

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

UNITHER LIQUID MANUFACTURING (Owner Number: 10091016)

Owner / Operator Contact Address

1,3 allee de la neste, COLOMIERS, FR-31 31770, FR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Caphosol

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LFD	Saliva, Artificial	Unknown	Class U	N/A	2024-06-25

Official Correspondent

No official correspondent registered.

US Agent Details

Danielle Seamon Email: Danielle.seamon@unither-pharma.com Phone: (240) 3552253

Related Public Records

Same Entity

UNITHER LIQUID MANUFACTURING

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 3007935577. Last updated year: 2026. Please use registration number 3007935577 when referencing this establishment in official correspondence.