Not currently registered with FDA under this name

Interdent, Inc.

Los Angeles, CA, United States. Named as applicant on 1 dental 510(k) clearance between 1998 and 1998. No establishment is registered with FDA under this exact name today.

Device types listed: 0
Brands and models: 0
510(k) clearances: 11998–1998
Markets registered in: 5111 registrations outside the US
Establishments: 0—

510(k) clearances per year, 1990–2026

Registered in 5 markets

Where regulators' registries name Interdent, 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	Interdent, Inc.	1 clearances	1998–1998	Below
Serbia	ALIMS	Manufacturer	Interdent d.o.o.	51	2023–2025	Pure Global AI
Saudi Arabia	SFDA	Manufacturer	INTERDENT d.o.o	43	—	Pure Global AI
South Korea	MFDS	Manufacturer	INTERDENT d.o.o.Interdent d.o.o.	16	2004–2009	Pure Global AI
Australia	TGA	Manufacturer	INTERDENT doo	1	2026–2026	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 Interdent, Inc. as the applicant.

Decided	510(k)	Device	Device type
27 Feb 1998	K972775	FASTDAM	EIE Rubber Dam

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.