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Straumann Standard Plus

Also known as: SP, Straumann Standard Plus Implant, Straumann Tissue Level SP

A parallel-walled tissue-level implant from Straumann with a 1.8 mm machined neck, using the synOcta connection on Regular Neck and Wide Neck platforms.

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Quick facts

Current statusCurrent. Standard Plus 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 1.8 mm, allowing flexible coronoapical placement with trans- or subgingival 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, available on Regular Neck (RN) and Wide Neck (WN) platforms. The ∅ 3.3 mm Narrow Neck CrossFit (NNC) variant is the exception: it is a Standard Plus implant with an internal CrossFit connection and its own NNC prosthetic components.Manufacturer-reported[1]
Platform switchingManufacturer documentation not located(The synOcta interface sits at the tissue-level shoulder; the documentation reviewed makes no platform-switching claim.)
Available diametersEndosteal diameter ∅ 3.3, 4.1 and 4.8 mm.Manufacturer-reported[1]
Available lengthsSP ∅ 3.3 mm RN and SP ∅ 3.3 mm NNC: 8–14 mm. SP ∅ 4.1 mm RN: 6–14 mm. In the ∅ 4.8 mm RN and WN rows the length cell is shared with the Standard implant, which is given as 6–14 mm (RN) and 6–12 mm (WN). A separate 4 mm Standard Plus Short implant is listed for open-end situations in the mandible with severely atrophic bone.Manufacturer-reported[1]

Overview

Standard Plus is the tissue-level implant most often chosen when the gum is thin or the site is anterior, because its polished collar is 1.8 mm rather than the 2.8 mm of the classic Standard implant. That single millimetre is very nearly the whole distinction between the two: body, thread and connection are otherwise the same. One genuine complication is that not every Standard Plus uses the same connection — the ∅ 3.3 mm Narrow Neck CrossFit variant carries a CrossFit interface and its own component range, so a laboratory told only "Standard Plus" can order the wrong parts. Straumann also lists a 4 mm Standard Plus Short implant for severely resorbed posterior mandibles, which is a distinct product rather than simply a short version of the standard one.

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 shorter 1.8 mm neck as offering additional options in the anterior maxilla where aesthetic demands are high, because it allows more flexible coronoapical placement than the 2.8 mm Standard neck.Manufacturer-reported

Further detail

Short implant optionThe Standard Plus 4 mm implant is described as Straumann’s shortest implant, combining a Standard Plus neck design, synOcta internal connection compatibility and a Bone Level thread to increase implant-to-bone contact.Manufacturer-reported[1]
Narrow implant optionThe Standard Plus ∅ 3.3 mm Narrow Neck CrossFit implant is described for narrow interdental spaces and bone ridges, with a minimal ridge width of 5.5 mm. Its body and thread design are the same as the ∅ 3.3 mm Bone Level NC implant.Manufacturer-reported[1]

Clinical evidence

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

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Popular comparisons

The clearances below are held by Straumann at brand level and cover its implant range, not Straumann Standard Plus 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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