Manufacturer registered with FDA

IPB Inc

Ogden, UT, United States. Lists 11 dental device types with FDA across 1 registered establishment.

FDA owner/operator10029225Contract manufacturerManufacturerRepacker / relabelerSpecification developer
Device types listed
11
Brands and models
4
510(k) clearances
0as applicant
Markets registered in
1United States
Establishments
1United States

Devices listed with FDA

What IPB Inc 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
Mouth Mirror
2024
Manual ToothbrushEFW · Class 1ToothbrushesMaker—2013
Intraoral Dental WaxEGD · Class 1—Lister
Dental Wax
2024
All Precision AttachmentEGG · Class 1—Maker—2020
Oral Cavity EvacuatorEHZ · Class 1Suction & evacuation unitsMaker
Evacuator
2023
Rubber DamEIE · Class 1Rubber dam systemsMaker—2020
Dental Retractor AccessoriesEIF · Class 1Dental hand instrumentsMaker—2020
Impression MaterialELW · Class 2Impression materialsMaker—2021
Dental FlossJES · Class 1Floss & interdental cleanersMaker
Floss, Dental
2024
Massaging PickJET · Class 1Floss & interdental cleanersMaker—2020
Endosseous Dental Implant AbutmentNHA · Class 2Implant abutmentsMaker—2022

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

IPB Inc 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: Innovative Product Brands, Inc. (1), Pac-Dent International, Inc. (1).

Decided510(k)DeviceApplicantDevice type
6 Jun 2022K220612PrimeLOC Attachment SystemInnovative Product Brands, Inc.NHA Endosseous Dental Implant Abutment
28 Jul 2015K151150ElementsPac-Dent International, Inc.ELW Impression Material

Registered establishments

EstablishmentLocationWhat it does
IPB IncFDA reg. 3003618527Ogden, UT, United StatesContract manufacturer, Manufacturer, Repacker / relabeler, Specification developer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10029225). 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.