Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3006990004

FEI Number

3006990004

Entity Name

Bioclear Matrix Systems, LLC

City/State/Country

Tacoma, WA, US

Establishment Address

3901 S Fife Street, Suite 100, Tacoma, WA 98409, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

Bioclear Matrix Systems, LLC (Owner Number: 9107200)

Owner / Operator Contact Address

3901 S Fife Street, Suite 100, Tacoma, WA 98409, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Black Triangle Gauge Evolve Matrix Height Indicator TwinRing Forceps Blasting Powder Magic Mix PrePolish Dual-Color Disclosing Solution TruContact True Contact 2 RockStar Sculpting and Polishing Discs Push-Pull Curved Micro Pliers Curved Sculpting Paddle TwinRing Sculpting Point Adjustable Push-Pull Scalpel Handle Clark Explorer Micro Hemostat Matrix Sculpting Scissors Esthetic Proportion Gauge/Contrastor Interproximal Carver RockStar Polisher Biofit Matrix Veneer 360 Matrix Evolve Matrix Bioclear Matrix BT Matrix TSS Matrix Magic Mix Cups

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
EIY	Instrument, Filling, Plastic, Dental	Dental	Class 1	872.4565	2011-02-21
EJG	Forceps, Rubber Dam Clamp	Dental	Class 1	872.6300	2018-12-27
EJR	Agent, Polishing, Abrasive, Oral Cavity	Dental	Class 1	872.6030	2018-12-27
DZP	Instrument, Diamond, Dental	Dental	Class 1	872.4535	2018-12-27
DZN	Instruments, Dental Hand	Dental	Class 1	872.4565	2007-09-14
JEP	Retainer, Matrix	Dental	Class 1	872.4565	2018-12-19
EHK	Cup, Prophylaxis	Dental	Class 1	872.6290	2023-12-08

Official Correspondent

Abigail Bowden

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Bioclear Matrix Systems, LLC

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
K121698	Dentsply International, Inc.	NUPRO SENSODYNE PROPHYLAXIS PASTE WITH NOVAMIN	2012-08-06
K831136	Almore Intl., Inc.	DOUBLE BOW TOOTH SEPARATOR	1983-06-08

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3006990004. Last updated year: 2026. Please use registration number 3006990004 when referencing this establishment in official correspondence.