Registered with FDA

Maxill Inc.

Cortland, OH, United States. Lists 23 dental device types with FDA across 1 registered establishment.

FDA owner/operator9042210Foreign exporterPrivate-label distributor
Device types listed
23
Brands and models
27
510(k) clearances
0as applicant
Markets registered in
3113 registrations outside the US
Establishments
1Canada

Registered in 3 markets

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

All markets
United States: 23 device types listedCanada: 109 registrationsColombia: 4 registrations
RegisteredHome: United StatesOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAListerMaxill Inc.23 device types—Below
CanadaHealth CanadaRegistration holderMAXILL INC.1091999–2026Pure Global AI
ColombiaINVIMARegistration holderMAXILL INC.MAXILL INC4—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 Maxill Inc. currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Dental Hand InstrumentsDZN · Class 1Dental hand instrumentsLister
Dental Wedges (Wooden, Plastic with Hole, Wedge Batons)
2015
Mouth MirrorEAX · Class 1Dental hand instrumentsLister
Maxill
2011
Articulation PaperEFH · Class 1—Lister
Maxill Articulating FilmMaxill Articulating FoilMaxill Articulating Paper
2015
Roll CottonEFN · Class 1—Lister
Maxill
2011
Over the Counter Denture CleanserEFT · Class 1Denture cleansers & adhesivesLister
Maxill
2011
Manual ToothbrushEFW · Class 1ToothbrushesLister
MAXILL
2000
Intraoral Dental WaxEGD · Class 1—Lister
Maxill
2011
Dental Contra- and Right-Angle Attachment HandpieceEGS · Class 1Dental handpiecesLister
Maxill
2012
Prophylaxis CupEHK · Class 1Polishing & prophylaxisLister
Maxill
2011
Preformed Impression TrayEHY · Class 1Impression traysLister
Impression Tray (Dual-Arch, Krystal Klear, Classic, Anodonita, Orthodontic)
2015
Restorative and Impression Material SyringeEID · Class 1Dental hand instrumentsLister
Maxill Dynamic Mixing TipsMaxill Dynamic Mixing Tips Intraoral ExtensionsMaxill Mixing Tips
2011
Rubber DamEIE · Class 1Rubber dam systemsLister
Maxill
2011
All Types RetractorEIG · Class 1Dental hand instrumentsLister
Cheek Retractors (Extraoral, Intraoral, Lip & Cheek, Single/Double Sided Hand Held)
2015
Polishing Agent WheelEJQ · Class 1Polishing & prophylaxisLister
Maxill
2011
Gutta-PerchaEKM · Class 1Root canal filling materialsLister
Maxill Gutta Percha Points
2015
Impression MaterialELW · Class 2Impression materialsLister
Maxill VPS Impression Material (Heavy Body, Light Body, Bite Registration, Monophase, Alginate)
2015
Periodontic ScalerEMN · Class 1Dental hand instrumentsLister
Maxill
2011
Dental FlossJES · Class 1Floss & interdental cleanersLister
Maxill
2000
Massaging PickJET · Class 1Floss & interdental cleanersLister
Maxill
2011
Disposable Fluoride TrayKMT · Class 1—Lister
Maxill
2011
Resin ApplicatorKXR · Class 1—Lister
Maxill
2011
Tongue ScraperLCN · Class 1—Lister
Maxill
2011
Accessories Operative Dental UnitNRD · Class 1—Lister
Maxill
2011

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

Maxill 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: Dmp, Ltd. (1), Team Technologies, Inc. (1).

Decided510(k)DeviceApplicantDevice type
13 Jan 2011K102836BONASIL A+ IMPRESSION MATERIALSDmp, Ltd.ELW Impression Material
16 May 1994K941189DISPOSABLE PROPHYLAXIS ANGLETeam Technologies, Inc.EGS Dental Contra- and Right-Angle Attachment Handpiece

Registered establishments

EstablishmentLocationWhat it does
MAXILL, INC.FDA reg. 3005558160ST. THOMAS Ontario, CanadaForeign exporter, Private-label distributor

Sources

FDA establishment registration & device listing (search FDA, owner/operator 9042210). 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.