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Anthogyr Axiom BL

Also known as: Axiom BL, Axiom Bone Level

A bone-level implant from Anthogyr with an extended, indexed three-lobed Morse taper connection of 2.7 mm diameter shared across every implant diameter.

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Quick facts

ManufacturerAnthogyr SAS, part of the Straumann Group since 2019Manufacturer-reported[1][2]
Implant levelBone level; Anthogyr colour-codes bone level packaging pink and tissue level greenManufacturer-reported[3]
Body geometryOffered in two profiles: Axiom REG (regular) and Axiom PXManufacturer-reported[1]
Thread designManufacturer documentation not located
Apex designManufacturer documentation not located
MaterialGrade V medical titanium, stated to comply with ASTM F136 and ISO 5832-3Manufacturer-reported[1]
SurfaceBCP — an osseoconductive surface treatment produced by biphasic calcium phosphate sandblastingManufacturer-reported[1]
ConnectionExtended, indexed three-lobed Morse taper connection with a 2.7 mm prosthetic emergence diameter and an M1.6 screw, identical on every implant diameterManufacturer-reported[3]
Platform switchingThe 2.7 mm prosthetic connection is narrower than every implant diameter offered, from Ø3.4 upwardsManufacturer-reported[3]
Available diametersØ3.4, 4.0, 4.6 and 5.2 mmManufacturer-reported[1][3]
Available lengths6.5, 8, 10, 12, 14, 16 and 18 mm depending on diameter; the Ø3.4 fixtures start at 8 mmManufacturer-reported[1]

Overview

Axiom BL’s defining feature is that the prosthetic connection is 2.7 mm on every implant, so a Ø3.4 mm and a Ø5.2 mm implant take exactly the same abutment. That simplifies stock and, more importantly for a patient, makes it likelier that a component will still be obtainable years later. The connection is a three-lobed indexed Morse taper rather than a hex, and the implant is made from grade 5 titanium alloy with a calcium-phosphate blasted surface — a different surface philosophy from the acid-etched finishes used by most of the systems it competes with. Anthogyr joined the Straumann Group in 2019, so Axiom is now sold through Straumann Group channels while remaining a distinct system.

Further detail

Narrow implant optionAnthogyr states that Ø3.4 mm implants are not recommended for single-tooth restorations in the molar regionManufacturer-reported[1]
Prosthetic ecosystemAxiom Multi Level provides compatibility between the Axiom BL and Axiom TL rangesManufacturer-reported[3]
Geographic availabilityRequires manual verification

Clinical evidence

We have not yet completed a system-specific evidence review for Anthogyr Axiom BL. 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 BL 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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