LIQUIDPRO US

FDA Device Registration & Listing · Santa Rosa, CA, US · Registration 3019585803

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
3019585803
FEI Number
3019585803
Entity Name
LIQUIDPRO US
City/State/Country
Santa Rosa, CA, US
Establishment Address
418 B. St. 4th floor, Santa Rosa, CA 95401, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
LiquidPro US (Owner Number: 10085592)
Owner / Operator Contact Address
418 B. St. 4th floor, Santa Rosa, CA 95401, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

EarPro

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NEC Bandage, Liquid, Skin Protectant General Hospital Class 1 880.5090 2022-07-09

Official Correspondent

Paul Dollar

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

LiquidPro US
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 3019585803. Last updated year: 2026. Please use registration number 3019585803 when referencing this establishment in official correspondence.
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