Not currently registered with FDA under this name

Xomed, Inc.

Arnold, MO, United States. Named as applicant on 1 dental 510(k) clearance between 1976 and 1976. No establishment is registered with FDA under this exact name today.

Device types listed: 0
Brands and models: 0
510(k) clearances: 11976–1976
Markets registered in: 321 registrations outside the US
Establishments: 0—

510(k) clearances per year, 1976–2026

Registered in 3 markets

Where regulators' registries name Xomed, 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	Xomed, Inc.	1 clearances	1976–1976	Below
South Korea	MFDS	Manufacturer	Xomed Inc.Xomed, Inc. · XOMED, INC · +2	16	1998–1999	Pure Global AI
Taiwan	TFDA	Manufacturer	XOMED CORPORATION	5	1977–1977	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 Xomed, Inc. as the applicant.

Decided	510(k)	Device	Device type
21 Sep 1976	K760570	ROBINSON MIDDLE EAR PROSTHESIS	EIB Irrigating (Dental) Syringe

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.