Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3004623350

FEI Number

3004623350

Entity Name

ASHTEL STUDIOS, INC.

City/State/Country

Ontario, CA, US

Establishment Address

1610 E Philadelphia st, Ontario, CA 91761, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

ASHTEL STUDIOS, INC. (Owner Number: 9094940)

Owner / Operator Contact Address

1610 E Philadelphia Street, --, Ontario, CA 91761, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Brush Buddies, Dental wax Brush Buddies, Tongue Cleaner Smart Care Dental probe Nosal suction SMART CARE SONICLEAN Dental Guard, Dental Tray Manual Toothbrush SMART CARE SONICLEAN Dental Hoe Soniclean Dental hand instrument Liquid dispenser

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
EGD	Wax, Dental, Intraoral	Dental	Class 1	872.6890	2021-01-19
EHA	Aligner, Beam, X-Ray	Dental	Class 1	872.1820	2008-10-09
LCN	Scraper, Tongue	Dental	Class 1	872.6855	2021-01-19
FQM	Bandage, Elastic	General Hospital	Class 1	880.5075	2021-01-19
EIX	Probe, Periodontic	Dental	Class 1	872.4565	2021-01-19
BSY	Catheters, Suction, Tracheobronchial	Anesthesiology	Class 1	868.6810	2021-01-19
MMD	Toothbrush, Ionic, Battery-Powered	Dental	Class 1	872.6865	2008-10-09
EHY	Tray, Impression, Preformed	Dental	Class 1	872.6880	2021-01-19
EFW	Toothbrush, Manual	Dental	Class 1	872.6855	2015-10-28
EMQ	Hoe, Periodontic	Dental	Class 1	872.4565	2021-01-19
JEQ	Toothbrush, Powered	Dental	Class 1	872.6865	2019-11-13
DZN	Instruments, Dental Hand	Dental	Class 1	872.4565	2021-01-19
KYX	Dispenser, Liquid Medication	General Hospital	Class 1	880.6430	2021-01-19

Official Correspondent

ANISH PATEL

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

ASHTEL STUDIOS, INC.

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
K973236	Procter & Gamble Co.	CREST TOOTHBRUSH WITH MICROSHIELD	1998-03-11

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3009171220	DENTIMED SAO JOAO	Sunrise, FL, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004623350. Last updated year: 2026. Please use registration number 3004623350 when referencing this establishment in official correspondence.