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Sign in to claim this brandAMERICAN TOOTH INDUSTRIES
US
Last updated May 23, 2026
What AMERICAN TOOTH INDUSTRIES makes
American Tooth Industries manufactures dental acrylic resins, temporary crown and bridge resins, and resin artificial teeth. Their product portfolio also includes reusable diamond dental burs, abrasive points, orthodontic wires, preformed metal denture clasps, and soft home-use denture reliners.
The company is based in the United States, and its products are categorized as Class I and Class II medical devices. These devices are listed within the FDA UDI database.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical products does American Tooth Industries manufacture?
American Tooth Industries produces a diverse range of dental supplies. Their primary offerings include dental acrylic resins, temporary crown and bridge resins, and resin artificial teeth. Additionally, they manufacture reusable diamond dental burs, abrasive points, orthodontic wires, preformed metal denture clasps, and soft home-use denture reliners. This variety allows them to support multiple aspects of dental restorative and orthodontic care.
Where is American Tooth Industries located?
American Tooth Industries is based in the United States. This location serves as the primary base for their manufacturing and operations regarding the dental devices they provide to the market.
How are the devices from American Tooth Industries classified?
The medical devices produced by American Tooth Industries are classified as either Class I or Class II. These classifications are determined by the regulatory framework governing medical devices, which categorizes products based on the level of risk and the regulatory controls necessary to ensure their safety and effectiveness.
Where can I find information about the devices manufactured by this company?
Information regarding the devices manufactured by American Tooth Industries can be found in the FDA UDI database. This registry is used to track medical devices, and the company lists its products there to ensure transparency and compliance with regulatory identification requirements.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
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- Website
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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 161532999
Catalogue (783)
Page 3 of 16| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Pyro Paquer | 070-11-0401/BR | FDA UDI | Class II | Active |
| Pyroplast Powder | 070-10-0404/67 | FDA UDI | Class II | Active |
| Pyroplast Powder | 070-10-0404/59 | FDA UDI | Class II | Active |
| Carbide Burrs | 013-19805 | FDA UDI | Class I | Active |
| Carbide Burrs | 013-19795 | FDA UDI | Class I | Active |
| Pourable Db | 072-50-0008 | FDA UDI | Class II | Active |
| Justi Imperial ViVO Posterior 1x4 X36U | 083-50-0620X36 | FDA UDI | Class II | Active |
| Ref Shade | 072-25-0009/67* | FDA UDI | Class II | Active |
| Pozzi Ortho Powder | 033-20033 | FDA UDI | Class II | Active |
| Lingual Bladed 1x16 33-D M A4 | 083-54-0001/A4 | FDA UDI | Class I | Active |
| Denture Base | 072-04-0008 | FDA UDI | Class II | Active |
| Pozzi Cobalt Clasp Wire In Spools | 015-410/7 | FDA UDI | Class I | Active |
| Namilon Powder | 070-20-0420/68 | FDA UDI | Class II | Active |
| Pozzi Cobalt Clasp Wire In Spools | 015-410/9 | FDA UDI | Class I | Active |
| Cut-Off Wheel | 010-19921/210 | FDA UDI | Class I | Active |
| C & B Formula | 070-40-0404/81 | FDA UDI | Class II | Active |
| Ortho Resin | 072-05-0004 | FDA UDI | Class II | Active |
| Pyroplast Powder | 070-10-0401/77 | FDA UDI | Class II | Active |
| Carbide Burrs | 016-19991-556 | FDA UDI | Class I | Active |
| Pozzi Ortho Liquid | 041-RP6132-01 | FDA UDI | Class II | Active |
| Justi- Pakto Powder | 070-28-0002/I | FDA UDI | Class II | Active |
| Repair Material | 072-06-0012 | FDA UDI | Class II | Active |
| Resin Cement Powder | 070-80-0400W | FDA UDI | Class II | Active |
| Pozzi Standard Wire Spools | 015-400/1.0 | FDA UDI | Class I | Active |
| Mounted Stones | 08-32084 M6 | FDA UDI | Class I | Active |
| Namilon Powder | 070-20-0420/65 | FDA UDI | Class II | Active |
| Abrasive Wheels | 08-39084 PW1 | FDA UDI | Class I | Active |
| Carbide Burrs | 016-19991-171 | FDA UDI | Class I | Active |
| Pozzi Ortho Liquid | 041-RP6131-01 | FDA UDI | Class II | Active |
| Pourable Db | 072-50-0005 | FDA UDI | Class II | Active |
| C & B Formula | 070-40-0404/60 | FDA UDI | Class II | Active |
| Carbide Burrs | 013-19797/L | FDA UDI | Class I | Active |
| Pyroplast Powder | 070-10-0401/IB | FDA UDI | Class II | Active |
| Justi- Pakto Powder | 070-28-0002/A3 | FDA UDI | Class II | Active |
| Pozzi Ortho Liquid | 041-RP6122-16 | FDA UDI | Class II | Active |
| Disc | 011-19941/309 | FDA UDI | Class I | Active |
| Ortho Resin | 072-05-0009 | FDA UDI | Class II | Active |
| Namilon Powder | 070-20-0401/IB | FDA UDI | Class II | Active |
| Carbide Burrs | 013-19796 | FDA UDI | Class I | Active |
| Justi- Pakto | 070-28-0004/P | FDA UDI | Class II | Active |
| Denture Base | 072-04-0034 | FDA UDI | Class II | Active |
| Frame Base | 072-07-0001 | FDA UDI | Class II | Active |
| Namilon Powder | 070-20-0404/65 | FDA UDI | Class II | Active |
| Justi Imperial ViVO Posterior 1x8 | 083-50-0620 | FDA UDI | Class II | Active |
| Denture Base | 072-04-0040 | FDA UDI | Class II | Active |
| Ref Shade | 072-25-0009/65* | FDA UDI | Class II | Active |
| Pyroplast Powder | 070-10-0404/77 | FDA UDI | Class II | Active |
| Disc | 011-19939/307 | FDA UDI | Class I | Active |
| Ortho Resin | 072-05-0017 | FDA UDI | Class II | Active |
| Pozzi Standard Wire In Spools | 015-400/1.1 | FDA UDI | Class I | Active |
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