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Sign in to claim this brandWhat Neoss, Ltd. makes
Neoss, Ltd. manufactures dental implant components, including permanent and temporary preformed suprastructures, two-piece screw endosteal implants, and single-use or reusable dental drill bits. Their portfolio also includes reusable instrument trays, surgical screwdrivers, and non-bioabsorbable pliable-polymer membranes for dental regeneration.
The company’s devices are classified under FDA regulations as Class I or Class II and are listed in the FDA’s Unique Device Identifier (UDI) database. Neoss, Ltd. is based in the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- neoss.com
- —
- —
- [email protected]
- Phone
- 999-999-9999
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 216693627
Catalogue (530)
Page 11 of 11| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Neoss Implant System | 41189 | FDA UDI | Class I | Unknown |
| Neoss Implant System | 51181 | EUDAMEDFDA UDI | Class I | Active |
| Neoss Implant System | 21229 | FDA UDI | Class II | Active |
| Neoss Implant System | 41140 | EUDAMEDFDA UDI | Class I | Active |
| Neoss Implant System | 31150 | FDA UDI | Class II | Unknown |
| Neoss Implant System | 41113 | FDA UDI | Class II | Active |
| Neoss Implant System | 41231 | EUDAMEDFDA UDI | Class II | Active |
| Neoss Implant System | 90141 | FDA UDI | Class I | Active |
| Neoss Implant System | 41187 | FDA UDI | Class I | Unknown |
| Yomi One Implant System | 24022 | FDA UDI | Class II | Active |
| Neoss Implant System | 21182 | FDA UDI | Class II | Active |
| Neoss Implant System | 41241 | EUDAMEDFDA UDI | Class II | Active |
| Neoss Implant System | 31170 | FDA UDI | Class I | Active |
| Neoss Implant System | 21251 | FDA UDI | Class II | Active |
| Neoss Implant System | 41153 | EUDAMEDFDA UDI | Class II | Active |
| Neoss Implant System | 90120 | FDA UDI | Class I | Active |
| Neoss Implant System | 31186 | FDA UDI | Class I | Active |
| Yomi One Implant System | 24011 | FDA UDI | Class II | Active |
| Yomi One Implant System | 24023 | FDA UDI | Class II | Active |
| Yomi One Implant System | 24012 | FDA UDI | Class II | Active |
| Neoss Proactive Tapered Implant | K113376 | FDA 510(k) | Class II | Active |
| Neoss Implant System 03.25 | K090452 | FDA 510(k) | Class II | Active |
| Membrane Screws and Membrane Tacks | K201561 | FDA 510(k) | Class II | Active |
| Neoss Access Abutments | K081851 | FDA 510(k) | Class II | Active |
| Neoss Ti Reinforced Membrane | K143327 | FDA 510(k) | Class II | Active |
| Neoss Individual Prosthetics | K211396 | FDA 510(k) | Class II | Active |
| Neoss TiBase, Neoss CoCr Abutments (Mono and Multi) | K150669 | FDA 510(k) | Class II | Active |
| Neoss Various Titanium Abutments | K071838 | FDA 510(k) | Class II | Active |
| Neo Implant System | K043195 | FDA 510(k) | Class II | Active |
| Neoss Proactive Implant | K083561 | FDA 510(k) | Class II | Active |
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