Manufacturer registered with FDA

CranioMandibular Rehab, Inc.

Wheat Ridge, CO, United States. Lists 2 dental device types with FDA across 1 registered establishment.

FDA owner/operator9026195ManufacturerSpecification developer
Device types listed
2
Brands and models
4
510(k) clearances
0as applicant
Markets registered in
34 registrations outside the US
Establishments
1United States

Registered in 3 markets

Where regulators' registries name CranioMandibular Rehab, Inc. as the manufacturer or the registration holder of a device.

All markets
United States: 2 device types listedEuropean Union: 2 registrationsUnited Kingdom: 2 registrations
RegisteredHome: United StatesOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAManufacturerCranioMandibular Rehab, Inc.2 device types—Below
European UnionEUDAMEDManufacturerCranioMandibular Rehab, Inc.2—Pure Global AI
United KingdomMHRAManufacturerCranioMandibular Rehab, Inc.2—Pure Global AI

Outside the US the count is of all the company's device registrations in that market, dental or not · matched by company name and country · registry data read 12 Nov 2026

Devices listed with FDA

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

Device typeCategoryRoleBrands and modelsListed since
Oral Irrigation UnitEFS · Class 1Oral irrigatorsMaker
Salvate
2019
Dental Retractor AccessoriesEIF · Class 1Dental hand instrumentsMaker
MBIOraMPAOraPlace
2025

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
CranioMandibular Rehab, Inc.FDA reg. 1723702Wheat Ridge, CO, United StatesManufacturer, Specification developer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 9026195). 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.