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Straumann Standard

Also known as: S, Straumann Standard Implant, Straumann Tissue Level

The classic parallel-walled tissue-level implant in the Straumann Dental Implant System, with a 2.8 mm machined neck and the synOcta connection.

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Quick facts

Current statusCurrent. The Standard implant is one of the implant lines described in Straumann’s Dental Implant System Basic Information.Manufacturer-reported[1]
Implant levelTissue level.Manufacturer-reported[1]
Body geometryParallel-walled endosteal body with a smooth machined neck section of 2.8 mm, intended for single-stage procedures in which the implant is not covered by soft tissue during healing.Manufacturer-reported[1]
Thread designThread pitch 1 mm on the ∅ 3.3 mm implant and 1.25 mm on all other diameters.Manufacturer-reported[1]
Apex designManufacturer documentation not located
MaterialRoxolid with the SLActive or SLA surface, or titanium with an SLA surface.Manufacturer-reported[1]
SurfaceSLActive or SLA.Manufacturer-reported[1]
ConnectionsynOcta — an internal Morse taper with an 8° cone and an octagon for repositioning prosthetic parts, on Regular Neck (RN, ∅ 4.8 mm) and Wide Neck (WN) platforms. Straumann also offers the Solid Abutment for this line.Manufacturer-reported[1]
Platform switchingManufacturer documentation not located
Available diametersEndosteal diameter ∅ 3.3, 4.1 and 4.8 mm.Manufacturer-reported[1]
Available lengthsS ∅ 3.3 mm RN: 8–16 mm. S ∅ 4.1 mm RN: 6–16 mm. S ∅ 4.8 mm RN: 6–14 mm. S ∅ 4.8 mm WN: 6–12 mm.Manufacturer-reported[1]

Overview

The Standard implant is the oldest surviving design in Straumann’s range and the reason many clinicians still associate the brand with a polished collar visible on a radiograph. Its 2.8 mm machined neck is intended to sit through the gum so that a second surgery to uncover the implant is unnecessary. The trade-off is aesthetic: in a thin-tissue anterior site that collar can show, which is precisely why the 1.8 mm Standard Plus exists. Prosthetically it is identical to Standard Plus, using the same synOcta 8° Morse taper with an octagonal index, so laboratories treat the two lines as one component system.

Technology

Clinical positioning

What the manufacturer says this system is designed for. This is not the same thing as independent clinical evidence, which is set out separately below.

Straumann describes the Standard implant as especially suitable for classic single-stage procedures, where the implant is placed at soft tissue level and left uncovered during healing.Manufacturer-reported

Clinical evidence

We have not yet completed a system-specific evidence review for Straumann Standard. Insufficient system-specific evidence How we grade evidence

Similar implant systems

Popular comparisons

The clearances below are held by Straumann at brand level and cover its implant range, not Straumann Standard specifically. We show them here because that is the level at which regulators actually issue them.

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) clearance30 records

Cleared as substantially equivalent to a predicate device. Not an FDA approval, and not a finding of safety or effectiveness.

NumberDeviceHolderDate
K252168Straumann® BLC Implants - Indication WideningInstitut Straumann AG2026-03-10
K250294Straumann® RidgeFit ImplantsInstitut Straumann AG2025-08-12
K241391Straumann® PURE Ceramic ImplantsInstitut Straumann AG2024-12-10
K234049Straumann® BLC and TLC Implants - Line extensionInstitut Straumann AG2024-03-20
K230108Straumann® BLC and TLC ImplantsInstitut Straumann AG2023-09-14
K223083Straumann SLActive labeling changesInstitut Straumann AG2023-06-22
K211052Straumann RidgeFit ImplantsInstitut Straumann AG2021-07-08
K210855Straumann BLX Implant SystemInstitut Straumann AG2021-06-21
K202942Straumann 4 mm Short ImplantsStraumann USA, LLC2021-02-08
K200586Straumann TLX Implant SystemInstitut Straumann AG2020-08-20
K191256Straumann BLX Ø3.5 mm ImplantsInstitut Straumann AG2019-12-27
K191895Straumann Mini ImplantsInstitut Straumann AG2019-12-09
K190662MRI Compatibility for Existing Straumann Dental Implant SystemsStraumann USA, LLC2019-06-17
K180477Straumann PURE Ceramic Implant SystemInstitut Straumann AG2019-01-04
K181703Straumann BLX Line Extension - Implants, SRAs and Anatomic AbutmentsInstitut Straumann AG2018-12-28
K173961Straumann BLX Implant SystemInstitut Straumann AG2018-06-05
K171784Straumann Dental Implant SystemStraumann USA, LLC2018-01-19
K171769Straumann PURE Ceramic ImplantsStraumann USA, LLC (On Behalf of Institut Straumann Ag)2017-11-14
K153758Straumann Bone Level Tapered ImplantsInstitut Straumann AG2016-03-23
K150938Straumann® Dental Implant System ¿ Roxolid® SLA ImplantsStraumann USA, LLC2015-07-24
K140878STRAUMANN BONE LEVEL TAPERED IMPLANTStraumann USA, LLC2014-08-20
K130222STRAUMANN DENTAL IMPLANT SYSTEMStraumann USA, LLC2013-04-29
K123784STRAUMANN DENTAL IMPLANT SYSTEMStraumann USA, LLC2013-04-10
K111357STRAUMANN NARROW NECK CROSSFIT (NNC) 03.3MM DENTAL IMPLANT SYSTEMStraumann USA2011-10-03
K093027STRAUMANN RC TEMPORARY ABUTMENTSStraumann USA2010-02-12
K083550STRAUMANN DENTAL IMPLANT SYSTEMStraumann USA2009-02-26
K081419STRAUMANN DENTAL IMPLANT SYSTEMInstitut Straumann AG2009-02-20
K060958STRAUMANN NARROW NECK IMPLANTSStraumann USA2006-08-24
K061176STRAUMANN DENTAL IMPLANTSInstitut Straumann AG2006-08-11
K033984STRAUMANN DENTAL IMPLANT SYSTEMInstitut Straumann AG2004-06-30

Other1 record

Of 100 records we inspected, 93 are supplied sterile, 7 are supplied non-sterile and 0 do not state it. MRI safety labelling: Labeling does not contain MRI Safety Information (52); MR Conditional (48). A UDI listing records what the manufacturer declared about the device; it is not a clearance or an approval.

NumberDeviceHolderDate
1219 device records—Straumann—

Clearance records for Straumann 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.

Sources

Numbers match the citations beside each claim above.

Primary sources

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