Straumann Group
Also known as: Straumann Holding AG, Institut Straumann AG
The Swiss corporate group that owns the Straumann, Neodent, Medentika and Anthogyr implant brands, listed on the SIX Swiss Exchange under the ticker STMN.
Key facts
| Headquarters | Basel, SwitzerlandVerified spec[1][2] |
|---|---|
| Country | SwitzerlandVerified spec[1] |
| Founded | Institut Straumann was founded in 1954 by Reinhard Straumann in Waldenburg, Switzerland; the business was refocused exclusively on dental implantology in 1990Verified spec[1] |
| Ownership | Publicly listed. Straumann Holding AG trades on the SIX Swiss Exchange under the ticker STMNVerified spec[2][1] |
| Brand | Implant brands: Straumann, Neodent, Medentika and Anthogyr. The wider group portfolio also includes ClearCorrect, NUVO, Alliedstar, Bay Materials, Createch, GalvoSurge, Straumann Ceramic, T-Plus and YllerVerified spec[1]Anthogyr SAS (Sallanches, France) and Medentika GmbH (Hügelsheim, Germany) are each listed at 100% ownership in the statutory group-companies table of the 2025 annual report |
| Manufacturer-described indication | Describes itself as a global leader in tooth replacement and orthodontic solutions, serving premium, challenger and value segments through separate brandsManufacturer-reported[2][1] |
| Geographic availability | Products and services available in more than 100 countriesManufacturer-reported[2] |
| manufacturingCountry | SwitzerlandVerified spec[3]Country of the FDA-registered device establishment, which may differ from the brand’s home country. |
Overview
Regulatory record
Read this before drawing conclusions. A clearance or certificate means a device may legally be sold in a market. It is not a finding that the implant performs well, and it is not a comparison against other implants. In particular, FDA "clearance" is not FDA "approval" — clearance means the FDA accepted the device as substantially equivalent to one already on the market. What these actually mean →
FDA 510(k) clearance154 records
Cleared as substantially equivalent to a predicate device. Not an FDA approval, and not a finding of safety or effectiveness.
| Number | Device | Holder | Date |
|---|---|---|---|
| K260460 | Neodent Gold Hue Custom Abutments, Medentika Custom Abutments Gold Hue | Institut Straumann AG | 2026-05-07 |
| K252168 | Straumann® BLC Implants - Indication Widening | Institut Straumann AG | 2026-03-10 |
| K253315 | Straumann Variobase Abutments XC for Bridge/Bar | Institut Straumann AG | 2026-01-22 |
| K250294 | Straumann® RidgeFit Implants | Institut Straumann AG | 2025-08-12 |
| K243278 | Custom Abutments | Institut Straumann AG | 2025-02-21 |
| K243478 | Straumann InLab Validated Workflow | Institut Straumann AG | 2025-02-19 |
| K241391 | Straumann® PURE Ceramic Implants | Institut Straumann AG | 2024-12-10 |
| K241575 | Straumann® Anatomic Healing Abutments XC (AHA) | Straumann USA, LLC | 2024-11-11 |
| K234049 | Straumann® BLC and TLC Implants - Line extension | Institut Straumann AG | 2024-03-20 |
| K230108 | Straumann® BLC and TLC Implants | Institut Straumann AG | 2023-09-14 |
| K223083 | Straumann SLActive labeling changes | Institut Straumann AG | 2023-06-22 |
| K222836 | Straumann® Variobase® Abutments and Straumann® n!ce® Zirconia discs | Institut Straumann AG | 2023-05-15 |
| K220878 | Straumann TLX Variobase C | Institut Straumann AG | 2022-06-16 |
| K220751 | Straumann BLX Temporary Abutment, VITA CAD-Temp, PMMA | Institut Straumann AG | 2022-06-02 |
| K213063 | TLX SRAs and TLX Gold Abutments | Institut Straumann AG | 2022-04-08 |
| K212533 | BLX WB Ø5.0 (L18), Ø5.5 and Ø6.5 mm (L14 and L16) Implants | Institut Straumann AG | 2022-01-28 |
| K203750 | Straumann CARES P-Series CAD/CAM System | Institut Straumann AG | 2021-10-09 |
| K211052 | Straumann RidgeFit Implants | Institut Straumann AG | 2021-07-08 |
| K203456 | Straumann CARES M-Series CAD/CAM System | Institut Straumann AG | 2021-06-23 |
| K210855 | Straumann BLX Implant System | Institut Straumann AG | 2021-06-21 |
| K201681 | Straumann Immediate Temporary Abutments | Institut Straumann AG | 2021-03-18 |
| K203355 | Straumann TLX Novaloc and Cementable Abutments | Institut Straumann AG | 2021-02-12 |
| K192742 | Straumann Variobase C | Institut Straumann AG | 2021-02-12 |
| K202942 | Straumann 4 mm Short Implants | Straumann USA, LLC | 2021-02-08 |
| K200586 | Straumann TLX Implant System | Institut Straumann AG | 2020-08-20 |
| K200597 | Straumann BLX Gold Abutments | Straumann USA, LLC (On Behalf of Institut Straumann Ag) | 2020-08-19 |
| K193046 | Straumann® Retentive System Novaloc TiN Abutments | Institut Straumann AG | 2020-08-13 |
| K192401 | Straumann Screw-Retained Abutments | Straumann USA, LLC | 2020-04-06 |
| K192893 | Straumann Ceramic Healing Abutments | Institut Straumann AG | 2020-01-03 |
| K191256 | Straumann BLX Ø3.5 mm Implants | Institut Straumann AG | 2019-12-27 |
| K191895 | Straumann Mini Implants | Institut Straumann AG | 2019-12-09 |
| K192029 | Straumann PUREloc abutments | Institut Straumann AG | 2019-10-28 |
| K190654 | Straumann CI RD Ceramic Healing Caps | Institut Straumann AG | 2019-06-28 |
| K190097 | Straumann CARES Screw-Retained Bridges and Bars | Institut Straumann AG | 2019-06-26 |
| K190662 | MRI Compatibility for Existing Straumann Dental Implant Systems | Straumann USA, LLC | 2019-06-17 |
| K190082 | Straumann BLX Variobase Abutment | Institut Straumann AG | 2019-04-17 |
| K190040 | Straumann BLX Line Extension - New Abutments | Institut Straumann AG | 2019-04-08 |
| K180477 | Straumann PURE Ceramic Implant System | Institut Straumann AG | 2019-01-04 |
| K181703 | Straumann BLX Line Extension - Implants, SRAs and Anatomic Abutments | Institut Straumann AG | 2018-12-28 |
| K173945 | Straumann SC Variobase Abutments | Institut Straumann AG | 2018-10-05 |
Showing the 40 most recent of 154. The full set is searchable in the authority's own database.
Other2 records
Registered device establishment in Switzerland. Registration records where a device is made or handled; it is not a clearance, an approval, or any assessment of the product.
| Number | Device | Holder | Date |
|---|---|---|---|
| 9613348 | — | INSTITUT STRAUMANN AG | — |
| 1219 device records | — | Straumann Group | — |
Clearance records for Straumann Group were retrieved from the issuing authority's own database, not from the manufacturer's marketing material. We attribute a clearance to a brand only when the filing holder belongs to that brand's corporate family — third-party clearances for compatible components are excluded, because they belong to the company that made the component, not to Straumann Group.
Sources
Numbers match the citations beside each claim above.
Primary sources
- [1]Straumann Group Annual Report 2025 — Straumann Holding AG, 2026. Accessed 2026-07-21.
- [2]Straumann Group Q1 2026 results media release — Straumann Holding AG, 2026. Accessed 2026-07-21.
- [3]openFDA — Device registrations and listings — US Food and Drug Administration. Accessed 2026-07-22.