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Sign in to claim this brandDentronix, Inc.
US
Last updated May 27, 2026
Information
- Country
- US
- Address
- —
- Website
- dentronix.com
- —
- —
- [email protected]
- Phone
- 330-916-7300
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 085690428
Catalogue (25)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Dentronix | D7107-01 | FDA UDI | Class II | Active |
| Dentronix | D7000CL | FDA UDI | Class II | Active |
| Dentronix | D7000F | FDA UDI | Class II | Active |
| Dentronix | DDS7000230 | FDA UDI | Class II | Active |
| Dentronix | DSSH-1 | FDA UDI | Class II | Active |
| Dentronix | DDS7000230K | FDA UDI | Class II | Active |
| Dentronix | DAD-BL | FDA UDI | Class II | Active |
| Dentronix | DDS7000115 | FDA UDI | Class II | Active |
| Dentronix | 60013947 | FDA UDI | Class II | Active |
| Dentronix | D7000C | FDA UDI | Class II | Active |
| Dentronix | 60013954 | FDA UDI | Class II | Active |
| Dentronix | D5000S-T | FDA UDI | Class II | Active |
| Dentronix | D5000S-HT | FDA UDI | Class II | Active |
| Dentronix | DAD-UL | FDA UDI | Class II | Active |
| Dentronix | D7000-SILVER | FDA UDI | Class II | Active |
| Dentronix | D7000M-S | FDA UDI | Class II | Active |
| Dentronix Model 2000 | K910202 | FDA 510(k) | Class II | Active |
| Modified Podiatry Products | K771006 | FDA 510(k) | Class I | Active |
| Dentronix Dds 5000 Dry Heat Sterilization System | K880322 | FDA 510(k) | Class II | Active |
| Nipper, Nail, P610 English | K770303 | FDA 510(k) | Class I | Active |
| New Podiatry Products | K771005 | FDA 510(k) | Class I | Active |
| Nipper, Pso4 Tissue | K770301 | FDA 510(k) | Class I | Active |
| Cutter, P605 General Purpose | K770304 | FDA 510(k) | Class I | Active |
| Cutter, P607 Bone | K770305 | FDA 510(k) | Class I | Active |
| Cutter, P606 Bone | K770302 | FDA 510(k) | Class I | Active |
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