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Anthogyr Axiom TL

Also known as: Axiom TL, Axiom Tissue Level

A tissue-level implant from Anthogyr with an integral transmucosal collar, offered on narrow and regular platforms and compatible with the Axiom bone-level prosthetic range through Axiom Multi Level.

Research in progress. Some fields on this entry are not yet verified against a primary source, so we have left them blank rather than filling them in — and this page is not published to search engines until they are.

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Quick facts

ManufacturerAnthogyr SAS, part of the Straumann Group since 2019Manufacturer-reported[1][2]
Implant levelTissue level; Anthogyr colour-codes tissue level packaging greenManufacturer-reported[3]
Body geometryOffered as Axiom TL REG and Axiom TL PX, with an integral collar above the implant bodyManufacturer-reported[3]
Thread designManufacturer documentation not located
Apex designManufacturer documentation not located
MaterialGrade V medical titanium, to ASTM F136 and ISO 5832-3Manufacturer-reported[1]
SurfaceBCP — biphasic calcium phosphate sandblasted osseoconductive surfaceManufacturer-reported[1]
ConnectionTwo connections: the inLink connection, a flat non-indexed lock-in fixation with an M2.8 thread for multiple-unit screw-retained work, and an indexed three-lobed M1.6 connection for single and multiple units; both on two platform diameters, narrow Ø4.0 mm and regular Ø4.8 mmManufacturer-reported[3]
Platform switchingManufacturer documentation not located
Available diametersØ3.4, 4.0, 4.6 and 5.2 mm across the Axiom rangeManufacturer-reported[1]
Available lengths6.5, 8, 10, 12, 14, 16 and 18 mm across the Axiom Multi Level rangeManufacturer-reported[1]

Overview

Axiom TL is the tissue-level half of Anthogyr’s system, meaning the implant carries its own polished collar through the gum rather than finishing at bone level. The name Axiom Multi Level, which appears on much of the documentation, refers to the fact that Anthogyr designed the tissue-level and bone-level implants to share a prosthetic ecosystem — that compatibility is the selling point rather than any single feature of the implant. Note that the TL platform diameters (Ø4.0 narrow and Ø4.8 regular) are a different measurement from implant body diameter, and the two are easy to confuse. We have recorded the diameter and length ranges at medium confidence because the surgical guide gives them for the Axiom range as a whole rather than for TL separately.

Further detail

Prosthetic ecosystemAxiom Multi Level is the range that provides compatibility between the tissue-level and bone-level systemsManufacturer-reported[3]
Geographic availabilityRequires manual verification

Clinical evidence

We have not yet completed a system-specific evidence review for Anthogyr Axiom TL. Insufficient system-specific evidence How we grade evidence

Similar implant systems

The clearances below are held by Straumann at brand level and cover its implant range, not Anthogyr Axiom TL 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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