BFFL Co LLC

FDA Device Registration & Listing · Port Chester, NY, US · Registration 3012971326

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
3012971326
FEI Number
3012971326
Entity Name
BFFL Co LLC
City/State/Country
Port Chester, NY, US
Establishment Address
36 Midland Ave, Port Chester, NY 10573, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
BFFL CO (Owner Number: 10052563)
Owner / Operator Contact Address
36 Midland Avenue, Port Chester, NY 10573, US
Initial Importer Flag
N
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
HEF Binder, Breast General Hospital Class 1 880.5160 2016-08-16

Official Correspondent

Elizabeth Chabner Thompson

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

BFFL CO
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 3012971326. Last updated year: 2026. Please use registration number 3012971326 when referencing this establishment in official correspondence.
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