Dental Device Guide
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Not currently registered with FDA under this name

Prometex, Inc.

Houston, TX, United States. Named as applicant on 2 dental 510(k) clearances between 1989 and 1990. No establishment is registered with FDA under this exact name today.

Device types listed
0
Brands and models
0
510(k) clearances
21989–1990
Markets registered in
1United States
Establishments
0—
1989: 11990: 119801990200020102020

510(k) clearances per year, 1980–2026

510(k) clearances

Clearances on which FDA names Prometex, Inc. as the applicant.

Decided510(k)DeviceDevice type
3 Apr 1990K900068ARISTEE (RESIN, CROWN AND BRIDGES)EBG Resin Temporary Crown and Bridge
24 Oct 1989K892710ARISTEE (TEMPORARY CROWN & BRIDGE RESIN)EBG Resin Temporary Crown and Bridge

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.