Dental Device Guide
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Not currently registered with FDA under this name

Aromacryl, LLC

Royal Oak, MI, United States. Named as applicant on 1 dental 510(k) clearance between 2002 and 2002. No establishment is registered with FDA under this exact name today.

Device types listed
0
Brands and models
0
510(k) clearances
12002–2002
Markets registered in
1United States
Establishments
0—
2002: 1200020102020

510(k) clearances per year, 2000–2026

510(k) clearances

Clearances on which FDA names Aromacryl, LLC as the applicant.

Decided510(k)DeviceDevice type
28 May 2002K021121AROMACRYLEBI Rebasing Repairing Relining Denture Resin

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.