Dental Device Guide
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Not currently registered with FDA under this name

Nortex USA, Inc.

Washington, DC, United States. Named as applicant on 1 dental 510(k) clearance between 1986 and 1986. No establishment is registered with FDA under this exact name today.

Device types listed
0
Brands and models
0
510(k) clearances
11986–1986
Markets registered in
1United States
Establishments
0—
1986: 119801990200020102020

510(k) clearances per year, 1980–2026

510(k) clearances

Clearances on which FDA names Nortex USA, Inc. as the applicant.

Decided510(k)DeviceDevice type
12 Mar 1986K854467S.T.P.B SOFT TISSUES PROTECTIVES BLADESEEJ Disk Guard

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.