Manufacturer registered with FDA

Xlent Global Inc

Santa Clara, CA, United States. Lists 5 dental device types with FDA across 1 registered establishment.

FDA owner/operator10087585Repacker / relabelerSpecification developer
Device types listed
5
Brands and models
0
510(k) clearances
0as applicant
Markets registered in
1United States
Establishments
1United States

Devices listed with FDA

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

Device typeCategoryRoleBrands and modelsListed since
Dental NeedleDZM · Class 1Dental needles & syringesMaker—2025
Dental Hand InstrumentsDZN · Class 1Dental hand instrumentsLister—2023
Dental Retractor AccessoriesEIF · Class 1Dental hand instrumentsLister—2025
Gutta-PerchaEKM · Class 1Root canal filling materialsLister—2023
Dental FlossJES · Class 1Floss & interdental cleanersLister—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
Xlent Global IncFDA reg. 3017181138Las Vegas, NV, United StatesRepacker / relabeler, Specification developer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10087585). 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.