PARNELL PHARMACEUTICALS, INC.

FDA Device Registration & Listing · SAN RAFAEL, CA, US · Registration 2936950

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
2936950
FEI Number
2936950
Entity Name
PARNELL PHARMACEUTICALS, INC.
City/State/Country
SAN RAFAEL, CA, US
Establishment Address
3070 Kerner Blvd Ste A, SAN RAFAEL, CA 94901, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
PARNELL PHARMACEUTICALS, INC. (Owner Number: 9092041)
Owner / Operator Contact Address
3070 Kerner Blvd. Ste A, San Rafael, CA 94901, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

MOUTH KOTE-R MOUTH KOTE Mouth Kote - MD Nomovid Pretz Preservative-free Nasal Spray Pretz (R) Saline Nasal Spray, Pretz Irrigation, Pretz Concentrate, Pretz Saline Refill

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LFD Saliva, Artificial Unknown Class U N/A 2006-11-17
KCJ Applicator, Ent Ear, Nose, Throat Class 1 874.5220 2012-12-08

Official Correspondent

FRANCIS PARNELL, MD

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

PARNELL 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 2936950. Last updated year: 2026. Please use registration number 2936950 when referencing this establishment in official correspondence.
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