Dental Device Guide
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Not currently registered with FDA under this name

Oracrew

Las Vegas, NV, United States. Named as applicant on 1 dental 510(k) clearance between 2016 and 2016. No establishment is registered with FDA under this exact name today.

Device types listed
0
Brands and models
0
510(k) clearances
12016–2016
Markets registered in
1United States
Establishments
0—
2016: 120102020

510(k) clearances per year, 2007–2026

510(k) clearances

Clearances on which FDA names Oracrew as the applicant.

Decided510(k)DeviceDevice type
26 Aug 2016K150830CompleClear Plastic Orthodontic Bracket and Wire ApplianceDYW Orthodontic Plastic Bracket

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.