NOVABAY PHARMACEUTICALS, INC

FDA Device Registration & Listing · Emeryville, CA, US · Registration 3006218807

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
3006218807
FEI Number
3006218807
Entity Name
NOVABAY PHARMACEUTICALS, INC
City/State/Country
Emeryville, CA, US
Establishment Address
2000 Powell Street, Suite 1150, Emeryville, CA 94608, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
NovaBay Pharmaceuticals, Inc (Owner Number: 10039889)
Owner / Operator Contact Address
2000 Powell Street, Ste. #1150, Emeryville, CA 94608, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
K143351
PMA Number
N/A

All Registered Proprietary Names

NeutroPhase PhaseOne Skin and Wound Cleanser intelliCase

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KMF Bandage, Liquid General Hospital Class 1 880.5090 2025-01-17
LRX Case, Contact Lens Ophthalmic Class 2 886.5928 2015-11-12

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

NovaBay Pharmaceuticals, 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 3006218807. Last updated year: 2026. Please use registration number 3006218807 when referencing this establishment in official correspondence.
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