Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3003130442

FEI Number

3003130442

Entity Name

BARON ANALYTICAL LABORATORIES LLC

City/State/Country

Milford, CT, US

Establishment Address

181 Research Drive, Unit 1, Milford, CT 06460, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Baron Analytical Laboratories LLC (Owner Number: 10089494)

Owner / Operator Contact Address

181 Research Drive, Unit 1, Milford, CT 06460, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
PHR	Diammine Silver Fluoride Dental Hypersensitivity Varnish	Dental	Class 2	872.3260	2023-12-15

Official Correspondent

Kevin Ovian

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Baron Analytical Laboratories LLC

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 3003130442. Last updated year: 2026. Please use registration number 3003130442 when referencing this establishment in official correspondence.