CARRASHIELD LABS, INC.

FDA Device Registration & Listing · Saint Petersburg, FL, US · Registration 3012121190

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
3012121190
FEI Number
3012121190
Entity Name
CARRASHIELD LABS, INC.
City/State/Country
Saint Petersburg, FL, US
Establishment Address
1876 Coffee Pot Blvd NE, Saint Petersburg, FL 33704, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
CarraShield Labs, Inc. (Owner Number: 10050469)
Owner / Operator Contact Address
1876 Coffee Pot Blvd NE, Saint Petersburg, FL 33704, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K150397
PMA Number
N/A

All Registered Proprietary Names

CarraShield Divine 9

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NUC Lubricant, Personal Obstetrics/Gynecology Class 2 884.5300 2015-11-20

Official Correspondent

Dean Fresonke

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

CarraShield Labs, Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K050212 Qualis, Inc. PERSONAL WARMING JELLY 2005-03-17

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3012121190. Last updated year: 2026. Please use registration number 3012121190 when referencing this establishment in official correspondence.
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