Registered with FDA

Swedent Dental Wholesale Group

West Valley, UT, United States. Lists 8 dental device types with FDA across 1 registered establishment.

FDA owner/operator10081704Repacker / relabeler
Device types listed
8
Brands and models
0
510(k) clearances
0as applicant
Markets registered in
1United States
Establishments
1United States

Devices listed with FDA

What Swedent Dental Wholesale Group currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Ultraviolet Activator for PolymerizationEBZ · Class 2Curing lightsLister—2021
Heat Source for Bleaching TeethEEG · Class 1Teeth whitening lightsLister—2021
Dental Air-Powered HandpieceEFB · Class 1Dental handpiecesLister—2021
Preformed Impression TrayEHY · Class 1Impression traysLister—2021
All Types RetractorEIG · Class 1Dental hand instrumentsLister—2021
Dental BurEJL · Class 1Dental burs & diamondsLister—2021
Ac-Powered Direct Drive HandpieceEKX · Class 1Dental handpiecesLister—2021
Dental Stain EraserMAU · 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

Also lists devices cleared under other names

Swedent Dental Wholesale Group lists these devices with FDA today. The clearance names a different applicant, as happens after a rename, an acquisition or a private-label agreement.

Original applicants: Foshan Cicada Dental Instrument Co, Ltd. (3).

Decided510(k)DeviceApplicantDevice type
12 Mar 2021K192649Endo MotorFoshan Cicada Dental Instrument Co, Ltd.EKX Ac-Powered Direct Drive Handpiece
13 Feb 2020K192233LED Curing LightFoshan Cicada Dental Instrument Co, Ltd.EBZ Ultraviolet Activator for Polymerization
9 Dec 2019K181900Dental high speed handpiece, Dental low speed handpieceFoshan Cicada Dental Instrument Co, Ltd.EFB Dental Air-Powered Handpiece

Registered establishments

EstablishmentLocationWhat it does
SWEDENT DENTAL WHOLESALE GROUPFDA reg. 3019381139Provo, UT, United StatesRepacker / relabeler

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10081704). 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.