Dental Device Guide
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Not currently registered with FDA under this name

Dental Manufacturing S.P.A

Littleton, CO, 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 Dental Manufacturing S.P.A as the applicant.

Decided510(k)DeviceDevice type
30 Jan 2002K013824ACRY PLUS, ACRY LUX, ACRY LUX V, ACRY ROCK, ACRY ROCK V AND Z-TONE PREFORMED PLASTIC DENTURE TEETHELM Teeth Plastic Denture

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.