Implant encyclopedia
Neobiotech® — implant systems
12 systems and 483 references in the DentGrow catalogue.
- Country
- South Korea
Neobiotech systems
| System | Connection | Ø | Length | Status |
|---|---|---|---|---|
| CMI Implant ISdesde 2012 | Internal Hex | 3.5–7 mm | 7.3–15 mm | In production |
| CMVI Implant IS II activedesde 2012 | Internal Hex | 3.5–7 mm | 7.3–15 mm | In production |
| IS-III activedesde 2018 | Internal Hex | 3.5–6 mm | 7.3–15 mm | In production |
| IS-III active S-Narrowdesde 2019 | Internal Hex | 3.2 mm | 8.5–15 mm | In production |
| IS-III active Shortdesde 2024 | Internal Hex | 5–6 mm | 6.6 mm | In production |
| IS-III HActivedesde 2018 | Internal Hex | 3.5–7 mm | 7.3–15 mm | In production |
| IT-III activedesde 2018 | Internal Octagon | 3.5–5 mm | 7–15 mm | In production |
| IT-III active Widedesde 2018 | Internal Octagon | 5–7 mm | 7–15 mm | In production |
| S-MiNidesde 2011 | Internal connection (other) | 2–3.5 mm | 8.5–15 mm | In production |
| S-MiNi Balldesde 2011 | Internal connection (other) | 2–3.5 mm | 8.5–15 mm | In production |
| SQ EBdesde 2009 | — | 3.5–6 mm | 7.3–13 mm | In production |
| SQ ITdesde 2009 | — | 3.5–5 mm | 8.5–15 mm | In production |
Official catalogues
- FDA 510(k) K232049 — IS-III active Short Implant · 2024
- FDA 510(k) K190849 — IS-III active System S-Narrow · 2019
- FDA 510(k) K173938 — IS-III HActive Fixture · 2018
- FDA 510(k) K181137 — IT-III active System · 2018
- FDA 510(k) K181138 — IS-III active System · 2018
- FDA 510(k) K113554 — CMI Implant IS System · 2012
- FDA 510(k) K120503 — Neo CMVI Implant IS II active · 2012
- FDA 510(k) K112540 — S-MiNi Implant System (peça única) · 2011
- FDA 510(k) K090377 — SQ EB System · 2009
- FDA 510(k) K090527 — SQ IT System · 2009
The links open the document on the manufacturer's website.
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.