Dental Device Guide
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Not currently registered with FDA under this name

Diamond General Development Corp.

Ann Arbor, MI, United States. Named as applicant on 1 dental 510(k) clearance between 1998 and 1998. No establishment is registered with FDA under this exact name today.

Device types listed
0
Brands and models
0
510(k) clearances
11998–1998
Markets registered in
1United States
Establishments
0—
1998: 11990200020102020

510(k) clearances per year, 1990–2026

510(k) clearances

Clearances on which FDA names Diamond General Development Corp. as the applicant.

Decided510(k)DeviceDevice type
17 Jul 1998DEN980003DIAMOND PROBE/PERIO 2000 SYSTEMMVH Sulfide Detection Device

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.