Manufacturer registered with FDA

D&S Dental Laboratory

Waunakee, WI, United States. Lists 1 dental device type with FDA across 1 registered establishment.

FDA owner/operator10088589ManufacturerRepacker / relabeler
Device types listed
1
Brands and models
24
510(k) clearances
0as applicant
Markets registered in
1United States
Establishments
1United States

Devices listed with FDA

What D&S Dental Laboratory currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Preformed CrownELZ · Class 1—Maker
E-MAX ANTERIOR ALL CERAMIC CROWNE-MAX ANTERIOR ALL CERAMIC CROWN SCANE-MAX POSTERIOR ALL-CERAMIC CROWNE-MAX POSTERIOR ALL-CERAMIC CROWN SCANLAB ZR MONOLITIC ZIRCONIA CROWN-FROM MODELLITHIUM DISILICATE ANTERIORLITHIUM DISILICATE ANTERIOR SCANMARYLAND BRIDGE EMAXMARYLAND BRIDGE EMAX SCANMARYLAND BRIDGE FULL ZIRCONIA
14 more
MARYLAND BRIDGE FULL ZIRCONIA SCANMARYLAND BRIDGE PFZ W/2 WINGSPFZPORCELAIN FUSED TO ZIRCONIA SCANZR CROWN-ZIRCONIA CROWNZR CROWN-ZIRCONIA CROWN SCANZR PLUS CROWNZR PLUS CROWN SCANZR Plus with Micro Layering-AnteriorZR Plus with Micro Layering-Anterior ScanZR Plus with Micro Layering-PosteriorZR Plus with Micro Layering-Posterior ScanZRV Zirconia CrownZRV Zirconia Crown Scan
2026

Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026

Registered establishments

EstablishmentLocationWhat it does
D&S DENTAL LABORATORYFDA reg. 3007484481Waunakee, WI, United StatesComplaint file establishment, Manufacturer, Repacker / relabeler

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10088589). 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.