Not currently registered with FDA under this name

American Dent-All, Inc.

Glendale, CA, United States. Named as applicant on 5 dental 510(k) clearances between 2000 and 2003. No establishment is registered with FDA under this exact name today.

Device types listed: 0
Brands and models: 0
510(k) clearances: 52000–2003
Markets registered in: 22 registrations outside the US
Establishments: 0—

510(k) clearances per year, 2000–2026

Registered in 2 markets

Where regulators' registries name American Dent-All, Inc. as the manufacturer or the registration holder of a device.

All markets

RegisteredHome: United StatesOne marker per market

Market	Regulator	Named as	Name on the registry	Registrations	Issued	Records
United States	FDA	Applicant	American Dent-All, Inc.	5 clearances	2000–2003	Below
Taiwan	TFDA	Manufacturer	AMERICAN DENT-ALL, INC.	2	2005–2005	Pure Global AI

Outside the US the count is of all the company's device registrations in that market, dental or not · matched by company name and country · registry data read 12 Nov 2026

510(k) clearances

Clearances on which FDA names American Dent-All, Inc. as the applicant.

Decided	510(k)	Device	Device type
17 Mar 2003	K030161	SUPERBOND	EJH Base Metal Alloy
6 Aug 2001	K011706	FLEXICAST PRIME	EJH Base Metal Alloy
3 Aug 2001	K011705	SUPREMCAST	EJH Base Metal Alloy
2 Jan 2001	K003509	FLEXICAST	EJH Base Metal Alloy
5 Jul 2000	K001383	SUPREMCAST V	EJH Base Metal Alloy

Sources

FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record of the most recent filing, which can be a US agent.