XPRESS BCD LLC

FDA Device Registration & Listing · Frederick, MD, US · Registration 3026674642

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
3026674642
FEI Number
3026674642
Entity Name
XPRESS BCD LLC
City/State/Country
Frederick, MD, US
Establishment Address
6024 White Flint Drive, Frederick, MD 21702, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
XPress BCD LLC (Owner Number: 10087201)
Owner / Operator Contact Address
6024 White Flint Drive, Frederick, MD 21702, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

XPress BCD

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
POY Post Breast Biopsy Hemostatic Breast Compression Device Radiology Class 2 892.1710 2023-03-08

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

XPress BCD 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 3026674642. Last updated year: 2026. Please use registration number 3026674642 when referencing this establishment in official correspondence.
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