Manufacturer registered with FDA

Applied Dental Inc DBA AD Surgical

Sunnyvale, CA, United States. Lists 4 dental device types with FDA across 1 registered establishment.

FDA owner/operator9040635Specification developer
Device types listed
4
Brands and models
16
510(k) clearances
0as applicant
Markets registered in
1United States
Establishments
1United States

Devices listed with FDA

What Applied Dental Inc DBA AD Surgical currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Mouth MirrorEAX · Class 1Dental hand instrumentsMaker
E&Pi-pak
2000
Periodontic ProbeEIX · Class 1Dental hand instrumentsMaker
E&P - Dental Double ended Explorer and Probei-pak,
2000
Operative ExplorerEKB · Class 1Dental hand instrumentsMaker
E&Pi pak
2000
Endosseous Dental Implant AccessoriesNDP · Class 1Implant instruments & surgical kitsMaker
Accu-StopEZ KeyEZ STENTEZ Stent Free-End SetEZ Stent Guided Step Drilling SetEZ Stent Multiple Teeth SetEZ Stent Single Tooth SetEZ StopperI-KEYThermoplastic Drill Template Set
2004

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
APPLIED DENTAL INC. DBA AD SurgicalFDA reg. 2954705Sunnyvale, CA, United StatesComplaint file establishment, Specification developer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 9040635). 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.