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Sign in to claim this brandPhoenix Dental, Inc.
US
Last updated May 30, 2026
What Phoenix Dental, Inc. makes
Phoenix Dental, Inc. manufactures professional and home-use dental coatings designed to desensitize teeth, including products such as Super Seal, Nanodent, and Phoenix Opti-Max Dental Implant with Plasma-Spray Titanium/Hydroxyapatite.
The company's devices are classified as Class II medical devices and are listed in the FDA 510(k) and FDA UDI registries; the manufacturer is based in the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What does Phoenix Dental, Inc. make?
Phoenix Dental, Inc. manufactures professional and home-use dental coatings designed to desensitize teeth, including products such as Super Seal, Nanodent, and Phoenix Opti-Max Dental Implant with Plasma-Spray Titanium/Hydroxyapatite, as stated in the provided device data summary.
Where is Phoenix Dental, Inc. based?
Phoenix Dental, Inc. is based in the United States, as indicated by the COUNTRY field in the device data, which specifies US as the country of origin for the manufacturer.
Which regulatory registries list Phoenix Dental, Inc.'s devices?
Phoenix Dental, Inc.'s devices are listed in the FDA 510(k) and FDA UDI registries, as explicitly stated in the LISTED IN field of the device data, which includes fda_510k and fda_udi as the registries where the devices are recorded.
How are Phoenix Dental, Inc.'s devices classified?
Phoenix Dental, Inc.'s devices are classified as Class II medical devices, as specified in the DEVICE CLASSES field of the device data, which indicates Class II as the classification level for the manufacturer's products.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- phoenixdental.com
- —
- —
- [email protected]
- Phone
- 877-463-9905
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 004701368
Catalogue (11)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Super Seal | 100298 | FDA UDI | Class II | Active |
| Super Seal | 100294 | FDA UDI | Class II | Active |
| Super Seal | 100290 | FDA UDI | Class II | Active |
| Nanodent | 0001 | FDA UDI | Class II | Active |
| Super Seal | 100295 | FDA UDI | Class II | Active |
| Super Seal | 100291 | FDA UDI | Class II | Active |
| Super Seal | K983477 | FDA 510(k) | Class II | Active |
| Discovred | K102821 | FDA 510(k) | Class II | Active |
| Phoenix Opti-Max Dent Impl W/Plas-Spray Tita/Hydro | K926101 | FDA 510(k) | Class II | Active |
| Super Seal Tooth Desensitizer | K120109 | FDA 510(k) | Class II | Active |
| Phoenix Opti-Max Dent Implant W/Plasma-Spray Titan | K926102 | FDA 510(k) | Class II | Active |
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