Dental Device Guide
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Registered with FDA

Bright Supply Inc

Canoga Park, CA, United States. Lists 17 dental device types with FDA across 1 registered establishment.

FDA owner/operator10078145
Device types listed
17
Brands and models
1
510(k) clearances
0as applicant
Markets registered in
1United States
Establishments
1United States

Devices listed with FDA

What Bright Supply Inc currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Saliva Ejector MouthpieceDYN · Class 1—Lister—2020
Dental NeedleDZM · Class 1Dental needles & syringesLister—2024
Dental Hand InstrumentsDZN · Class 1Dental hand instrumentsLister—2021
Resin Impression Tray MaterialEBH · Class 1Impression traysLister
Britedent
2020
Air and/or Water Syringe UnitECB · Class 1Dental hand instrumentsLister—2020
Roll CottonEFN · Class 1—Lister—2020
Prophylaxis CupEHK · Class 1Polishing & prophylaxisLister—2021
Oral Cavity EvacuatorEHZ · Class 1Suction & evacuation unitsLister—2020
Irrigating (Dental) SyringeEIB · Class 1Dental hand instrumentsLister—2020
Irrigating Endodontic Periodontic SyringeEIC · Class 1Dental hand instrumentsLister—2021
Restorative and Impression Material SyringeEID · Class 1Dental hand instrumentsLister—2021
Dental BurEJL · Class 1Dental burs & diamondsLister—2023
Endodontic Pulp Canal FileEKS · Class 1Endodontic filesLister—2020
Endodontic BroachEKW · Class 1Endodontic filesLister—2020
Mechanical Denture CleanerJER · Class 1Denture cleansers & adhesivesLister—2023
Paper Saliva AbsorberKHR · Class 1—Lister—2020
Resin ApplicatorKXR · Class 1—Lister—2021

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
BRIGHT SUPPLY INCFDA reg. 3017498782Canoga Park, CA, United StatesComplaint file establishment

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10078145). 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.