Implant encyclopedia
Keystone Dental® — implant systems
19 systems (1 discontinued) and 475 references in the DentGrow catalogue.
- Country
- United States
Keystone Dental systems
| System | Connection | Ø | Length | Status |
|---|---|---|---|---|
| Ex Hex (corpo padrão) — Southern Implants®Platforms: Ø3.25 mm (hex 2.54), Ø3.75 mm (hex 2.70), Ø4.0 mm (hex 2.70), Ø5.0 mm (hex 2.70), Ø6.0 mm (hex 2.70)Made by Southern Implants® | External Hex | 3.25–6 mm | 6–18 mm | In production |
| Ex Hex MAX (molar) — Southern Implants®Made by Southern Implants® | External Hex | 7–9 mm | 7–11 mm | In production |
| Ex Hex Zigomático 55° — Southern Implants®Made by Southern Implants® | External Hex | 4.3 mm | 35–60 mm | In production |
| Genesis ACTIVE™desde 2023 | Internal Hex | 3.5–5.5 mm | 8.5–16 mm | In production |
| Genesis® (TiLobe®)Platforms: Ø3.5/3.8 mm, Ø4.5 mm, Ø5.5/6.5 mmdesde 2010 | Internal connection (other) | 3.5–6.5 mm | 8.5–16 mm | In production |
| MOLARIS I-HEXMRT™Platforms: Ø5.7 mm (implante Ø7.0), Ø6.5 mm (implante Ø8.0), Ø7.5 mm (implante Ø9.0) | Internal Hex | 7–9 mm | 7–11 mm | In production |
| MOLARIS TiLobeMAXX™Platforms: Ø5.7 mm (implante Ø7.0), Ø6.5 mm (implante Ø8.0), Ø7.5 mm (implante Ø9.0) | Internal connection (other) | 7–9 mm | 7–11 mm | In production |
| Oct (Octógono Interno) — Southern Implants®Platforms: Ø3.3 mm, Ø4.0 mm, Ø4.8 mm, Ø5.7 mmMade by Southern Implants® | Internal Octagon | 3.3–5.7 mm | 6–14 mm | In production |
| Oct MAXIT™ (molar) — Southern Implants®Platforms: Ø4.8 mm (implante Ø7.0), Ø6.5 mm (implantes Ø8.0 e Ø9.0)Made by Southern Implants® | Internal Octagon | 7–9 mm | 7–11 mm | In production |
| Prima Plus™ (TiLobe®) | Internal connection (other) | 3.5–6 mm | 8–15 mm | In production |
| Prima Plus™ ConicalPlatforms: Ø3.25 mm (implante Ø3.5), Ø3.71 mm (implante Ø4.1), Ø4.47 mm (implante Ø5.0), Ø5.50 mm (implante Ø6.0)desde 2024 | Internal Hex | 3.5–6 mm | 8–15 mm | In production |
| PrimaConnex® (TiLobe®)Platforms: Ø3.5 mm (SD), Ø4.1 mm (RD), Ø5.0 mm (WD)desde 2005 | Internal connection (other) | 3.3–5 mm | 8–15 mm | In production |
| PrimaSolo® (peça única)desde 2005 | Internal connection (other) | 3–5 mm | 10–15 mm | In production |
| Restore® (External Hex)Platforms: Ø3.3 mm (SD), Ø4.1 mm (RD), Ø5.0 mm (WD)desde 1994 | External Hex | 3.3–6 mm | 6–15 mm | In production |
| Stage-1® (tissue level)Platforms: Ø4.8 mm (RDS — Regular Diameter), Ø6.5 mm (WDS — Wide Diameter)desde 2001 | Morse Taper | 3.3–6.3 mm | 8–16 mm | In production |
| Tri-Max® (molar) — Southern Implants®Made by Southern Implants® | Internal Hex | 7–9 mm | 7–11 mm | In production |
| Tri-Nex® — Southern Implants®Platforms: Ø3.5 mm, Ø4.3 mm, Ø5.0 mm, Ø6.0 mmMade by Southern Implants® | Internal Hex | 3.5–6 mm | 8.5–16.5 mm | In production |
| Z-Max | — | 7–9 mm | 7–11 mm | In production |
| Renova® (Internal Hex)2003– | Internal Hex | 3.75–4.75 mm | — | Discontinued |
Official catalogues
- Páginas de produto do fabricante — TiLobe®, Prima Plus, Genesis e Molaris (referência a referência, com Ø, comprimento e conexão) · 2026
- Registo de estabelecimento FDA nº 3011936113 (Keystone Dental Inc.) — lista os 510(k) da Southern Implants, Inc. distribuídos pela Keystone · 2026
- FDA 510(k) K240966 — Prima Plus Conical Implant System · 2024
- Catálogo PrimaConnex® & PrimaSolo® — MK40012 Rev M · 2023
- FDA 510(k) K223814 — Genesis ACTIVE Implant System · 2023
- Manual protético RESTORE® — MK40041 Rev C · 2018
- Manual protético STAGE-1 (Keystone Dental) — conexões RDS/WDS e compatibilidade Straumann® · 2016
- FDA 510(k) K101545 — Genesis Implant System · 2010
- FDA 510(k) K072768 — Restore, Stage-1, Renova, PrimaSolo e PrimaConnex (modificação de superfície) · 2007
- Patente US7249949B2 «Internal connection dental implant» — titular Keystone Dental Inc. · 2007
- FDA 510(k) K050506 — PrimaSolo One-Piece Implants & Healing Caps · 2005
- FDA 510(k) K051614 — PrimaConnex Internal Connection Implant System · 2005
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The brand and product names mentioned here belong to their respective owners and are used for identification only. DentGrow has no connection with these manufacturers and is not sponsored or endorsed by them.
Technical information is indicative and intended to help with identification. It does not replace the packaging, the clinical record or the manufacturer's catalogue, which always prevails. Found an error? Let us know via Manufacturers' catalogues.
Some of the data comes from AccessGUDID, a public database of the National Library of Medicine (NLM), National Institutes of Health, Department of Health and Human Services. The NLM is not responsible for this product and does not endorse or recommend it. Other data comes from EUDAMED (© European Union), reused under the CC BY 4.0 licence, with changes.