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Sign in to claim this brandDENTSPLY IH, INC.
US
Last updated May 24, 2026
What DENTSPLY IH, INC. makes
Dentsply IH, Inc. manufactures transgingival implants, permanent preformed dental implant suprastructures, and custom-made dental implantation drilling templates. The company also produces single-use surgical drill guides, custom-made surgical guide kits for bone anatomy, temporary dental crowns and bridges, and ceramic dental bridges.
The company is based in the United States and maintains a portfolio consisting of Class I and Class II medical devices. These products are listed in 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
Where is Dentsply IH, Inc. based?
Dentsply IH, Inc. is based in the United States. This information is provided to clarify the company's primary location of operations as stated in the official device registry data.
What types of medical devices does Dentsply IH, Inc. manufacture?
The company manufactures a range of dental products including transgingival implants, permanent preformed dental implant suprastructures, and custom-made dental implantation drilling templates. They also produce single-use surgical drill guides, custom-made surgical guide kits for bone anatomy, temporary dental crowns and bridges, and ceramic dental bridges. This list reflects the specific product categories identified in the company's registry profile.
How are the devices from Dentsply IH, Inc. classified?
The medical devices produced by Dentsply IH, Inc. are classified as Class I and Class II. This classification system is used to categorize devices based on the level of regulatory control required, as indicated in the provided device data.
Where can I find a list of devices from this manufacturer?
Devices from Dentsply IH, Inc. are listed in the FDA UDI database. This registry is the official source used to track the specific medical devices manufactured by the company.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- dentsply.com
- —
- —
- [email protected]
- Phone
- +1(800)531-3481
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 847337201
Catalogue (58)
Page 1 of 2| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Atlantis | Atl BridgeBase Ti AM | FDA UDI | Class II | Active |
| Mguide® | MG-STN3 | FDA UDI | Class I | Active |
| Atlantis™ | 35505 | FDA UDI | Class II | Active |
| Mguide® | MG-STN5 | FDA UDI | Class I | Active |
| Atlantis | 36416 | FDA UDI | Class II | Active |
| Atlantis™ | 36456 | FDA UDI | Class II | Active |
| Atlantis™ | 36352 | FDA UDI | Class II | Active |
| Atlantis® | 35011 | FDA UDI | Class I | Active |
| Atlantis™ | 35517 | FDA UDI | Class II | Active |
| Atlantis™ | 35304 | FDA UDI | Class II | Active |
| Atlantis™ | 36452 | FDA UDI | Class II | Active |
| Atlantis™ | 35355 | FDA UDI | Class II | Active |
| Mguide® | MG-STN4 | FDA UDI | Class I | Active |
| Mguide® | MG-STN7 | FDA UDI | Class I | Active |
| Atlantis™ | 35402 | FDA UDI | Class II | Active |
| Atlantis® | 35030 | FDA UDI | Class I | Active |
| Mguide® | MG-STN2 | FDA UDI | Class I | Active |
| Atlantis® | 36331 | FDA UDI | Class II | Active |
| Atlantis™ | 35515 | FDA UDI | Class II | Active |
| Atlantis™ | 35502 | FDA UDI | Class II | Active |
| Atlantis™ | 36406 | FDA UDI | Class II | Active |
| Atlantis™ | 35040 | FDA UDI | Class II | Active |
| Atlantis® | 36332 | FDA UDI | Class II | Active |
| Simplant® | 54500228 | FDA UDI | Class I | Active |
| Atlantis™ | 35352 | FDA UDI | Class II | Active |
| Atlantis™ | 35401 | FDA UDI | Class II | Active |
| Atlantis | 36466 | FDA UDI | Class II | Active |
| Simplant | Version 18 | FDA UDI | Class II | Unknown |
| Atlantis™ | 35413 | FDA UDI | Class II | Active |
| Atlantis™ | 36362 | FDA UDI | Class II | Active |
| Atlantis™ | 36306 | FDA UDI | Class II | Active |
| Atlantis™ | 35504 | FDA UDI | Class II | Active |
| Atlantis™ | 35503 | FDA UDI | Class II | Active |
| Atlantis™ | 35501 | FDA UDI | Class II | Active |
| Atlantis™ | 35518 | FDA UDI | Class II | Active |
| Atlantis | 36302 | FDA UDI | Class II | Active |
| Mguide® | MG-STN1 | FDA UDI | Class I | Active |
| Atlantis | 36462 | FDA UDI | Class II | Active |
| Atlantis™ | 36402 | FDA UDI | Class II | Active |
| Atlantis™ | 35404 | FDA UDI | Class II | Active |
| Atlantis™ | 36352 | FDA UDI | Class II | Active |
| Mguide® | MG-STN8 | FDA UDI | Class I | Active |
| Atlantis™ | 35020 | FDA UDI | Class II | Active |
| Simplant® | 54500220 | FDA UDI | Class I | Active |
| Atlantis® | 36333 | FDA UDI | Class II | Active |
| Atlantis™ | 35417 | FDA UDI | Class II | Active |
| Atlantis™ | 35415 | FDA UDI | Class II | Active |
| Atlantis | 36362 | FDA UDI | Class II | Active |
| Atlantis™ | 35353 | FDA UDI | Class II | Active |
| Atlantis™ | 35511 | FDA UDI | Class II | Active |
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