Registered with FDA

Gregory Weil Dental Ceramic Studio, Inc.

Chico, CA, United States. Lists 3 dental device types with FDA across 1 registered establishment.

FDA owner/operator10091546Repacker / relabeler
Device types listed
3
Brands and models
3
510(k) clearances
0as applicant
Markets registered in
1United States
Establishments
1United States

Devices listed with FDA

What Gregory Weil Dental Ceramic Studio, Inc. currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Posterior with Metal Insert Artificial TeethELJ · Class 1—Lister
Metal Insert For Dental Prosthetic
2024
Teeth Plastic DentureELM · Class 2Denture resins & teethLister
Denture
2024
Preformed CrownELZ · Class 1—Lister
Crown
2024

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
GREGORY WEIL DENTAL CERAMIC STUDIO, INC.FDA reg. 3012968498Chico, CA, United StatesRepacker / relabeler

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10091546). 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.