Data / Medical devices / United States / Beaming White LLC

Beaming White LLC: FDA-registered device maker in Vancouver, WA, United States, 1 510(k) clearance

Name: Beaming White LLC FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Beaming White LLC is registered with the FDA (registration 3007060769) in Vancouver, WA, United States. It lists 18 device types. The FDA files 1 510(k) clearance under its listings, the newest dated November 1, 2013. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number: 3007060769
Address: 1205 NE 95th St Ste A, Vancouver, WA, United States, 98665
Owner or operator: Beaming White LLC (10031912)
Roles: Manufacturer, Repackager or relabeler
First device listed: March 20, 2010
Registered through: 2026
Brand names listed: Advanced kit, Beaming White, Beaming White Take-home kit, Dental Gum Dam, Dental swabs, Facial Bed, Forever White Headset kit, Forever White pen and more

Devices it lists

Device	Product code	Class	Role	Source
Aligner, Sequential	NXC	2	Repackager or relabeler	accessdata.fda.gov
Chair, Adjustable, Mechanical	INN	1	Repackager or relabeler	accessdata.fda.gov
Chair, Examination And Treatment	FRK	1	Repackager or relabeler	accessdata.fda.gov
Cleanser, Denture, Over The Counter	EFT	1	Repackager or relabeler	accessdata.fda.gov
Dam, Rubber	EIE	1	Repackager or relabeler	accessdata.fda.gov
Eraser, Dental Stain	MAU	1	Manufacturer	accessdata.fda.gov
Heat Source For Bleaching Teeth	EEG	1	Manufacturer	accessdata.fda.gov
Instrument, Filling, Plastic, Dental	EIY	1	Repackager or relabeler	accessdata.fda.gov
Material, Impression Tray, Resin	EBH	1	Repackager or relabeler	accessdata.fda.gov
Needle, Dental	DZM	1	Repackager or relabeler	accessdata.fda.gov
Protector, Dental	BRW	1	Repackager or relabeler	accessdata.fda.gov
Retractor, All Types	EIG	1	Repackager or relabeler	accessdata.fda.gov
Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear)	HOY	1	Repackager or relabeler	accessdata.fda.gov
Strip, Polishing Agent	EHM	1	Repackager or relabeler	accessdata.fda.gov
Syringe, Irrigating (Non Dental)	KYZ	1	Repackager or relabeler	accessdata.fda.gov
Toothbrush, Powered	JEQ	1	Repackager or relabeler	accessdata.fda.gov
Tray, Impression, Preformed	EHY	1	Repackager or relabeler	accessdata.fda.gov
Unit, Oral Irrigation	EFS	1	Repackager or relabeler	accessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided	510(k) number	Device	Product code	Decision	Applicant	Source
November 1, 2013	K123514	CLEARPATH ALIGNER	NXC	Substantially Equivalent	Qserve America, Inc.	accessdata.fda.gov

Compare with other makers

Updated November 1, 2013. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.