BC3 TECHNOLOGIES

FDA Device Registration & Listing · Baltimore, MD, US · Registration 3026322855

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
3026322855
FEI Number
3026322855
Entity Name
BC3 TECHNOLOGIES
City/State/Country
Baltimore, MD, US
Establishment Address
3701 A Southwestern Blvd, suite 100, Baltimore, MD 21229, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
BC3 Technologies (Owner Number: 10087277)
Owner / Operator Contact Address
3701 A Southwestern Blvd, Baltimore, MD 21229, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K210751
PMA Number
N/A

All Registered Proprietary Names

seal

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
QSY Hemostatic Wound Dressing Without Thrombin Or Other Biologics Unknown Class U N/A 2023-02-07

Official Correspondent

Wayne Grube

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

BC3 Technologies
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
K220566 Koag, LLC Vascette HP (hemostatic pad) 2022-07-29
K080818 Hem Con Medical Technologies, Inc. HEMCON BANDAGE, HEMCON BANDAGE OTC, HEMCON CHITOFLEX-SURGICAL DRESSING 2008-05-15
K893123 Les Laboratorires Brothier, S.A. ADHESIVE BANDAGES & PADS FOR MINOR CUTS/SCRAPES 1990-02-13
K143462 Benq Materials Corporation AnsCare ChitoClot Gauze (prescription use), AnsCare ChitoClot Gauze (over-the-counter use) 2015-05-08
K040208 Tz Medical, Inc. NEPTUNE PAD, NEPTUNE DISC, NEPTUNE COMFORT-BAND, COMFORT-BAND 2004-05-11

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3026322855. Last updated year: 2026. Please use registration number 3026322855 when referencing this establishment in official correspondence.
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