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Anthogyr Sas

France FR-MF-000000602 Last updated 22 Oct 2026 Part of anthogyr

Devices
837
Registries
EUDAMEDGUDIDFDA 510(k)
FDA recalls
0

Catalogue837

Page 7 of 17

  • HECA002_6 Ref HECA002_6

    Class I EUDAMED Active

  • Anthofit Ref HEAN001

    Class I EUDAMED Active

  • Mini Implant Ref INMODMIO

    Class IIa EUDAMED Active

  • 153-41-SA Ref 153-41-SA

    Class I EUDAMED Active

  • 12041 Ref 12041

    Class I EUDAMED Active

  • 5493 Ref 5493

    Class I EUDAMED Active

  • 155-35-SA Ref 155-35-SA

    Class I EUDAMED Active

  • 151-02-Kit Ref 151-02-KIT

    Class I EUDAMED Active

  • inLink Ref IL-TOOL2

    Class I EUDAMED Active

  • 4756 Ref 4756

    Class I EUDAMEDFDA UDI Active

  • Aatool-4 Ref AATOOL-4

    Class I EUDAMED Active

  • HECA004_6 Ref HECA004_6

    Class I EUDAMED Active

  • 5475 Ref 5475

    Class I EUDAMED Active

  • Inmodcpv Ref INMODCPV

    Class I EUDAMED Active

  • 5608_Q Ref 5608_Q

    Class I EUDAMED Active

  • 5492 Ref 5492

    Class I EUDAMED Active

  • Inlink Ref ILL100T-4

    Class I EUDAMED Active

  • Inexmost Ref INEXMOST

    Class I EUDAMED Active

  • Aatool-M Ref AATOOL-M

    Class I EUDAMED Active

  • 5490 Ref 5490

    Class I EUDAMED Active

  • inLink Ref ILL300

    Class I EUDAMED Active

  • Inmoico Ref INMOICO

    Class I EUDAMED Active

  • 11795-X Ref 11795-X

    Class I EUDAMED Active

  • 10415 Ref 10415

    Class I EUDAMED Active

  • Inlink Ref ILLG100-2

    Class IIb EUDAMED Active

  • First Drill Ref OPGS20

    Class IIa EUDAMEDFDA UDI Active

  • Axin Ref AXIN-C-40-10

    Class IIb EUDAMED Active

  • Inlink Ref ILC100T-R

    Class IIb EUDAMED Active

  • First Drill Ref OPFP20

    Class I EUDAMEDFDA UDI Active

  • Anthogyr Implanteo Implantology And Dental Surgical Motor Unit Ref K102241

    Class I FDA 510(k) Active

  • Anthofit Oi, Anthofit He, Ossfit And Axiom Ref K101913

    Class II FDA 510(k) Active

  • Axiom PX Ref K161177

    Class II FDA 510(k) Active

  • Axiom Reg Ref K131066

    Class II FDA 510(k) Active

  • Montblanc Surgical Contra-Angle And Straight Handpiece Ref K111532

    Class I FDA 510(k) Active

  • Axiom Ref OPAT331

    Class IIb EUDAMEDFDA UDI Active

  • Axiom Ref XT64120

    Class IIb EUDAMEDFDA UDI Active

  • Axiom Ref AX15227B41-ET

    Class IIb EUDAMED Active

  • Mont Blanc Ref 10476

    Class I EUDAMED Active

  • Axiom Ref OPHS410

    Class IIb EUDAMEDFDA UDI Active

  • Axiom Ref TOP40080R2

    Class IIb EUDAMED Active

  • Axiom Ref PXFC_NOT

    Class I EUDAMEDFDA UDI Active

  • Axiom Ref TXT40100R1

    Class IIb EUDAMED Active

  • Axiom Ref OPAT41-7

    Class IIb EUDAMEDFDA UDI Active

  • Axiom Ref OPHS520

    Class IIb EUDAMEDFDA UDI Active

  • Axiom Ref TOP40060R3

    Class IIb EUDAMED Active

  • Axiom Ref OPAT540

    Class IIb EUDAMEDFDA UDI Active

  • Axiom Ref OPSHSB34

    Class IIb EUDAMED Active

  • Axiom Ref OPFLEX436-AA

    Class IIb EUDAMED Active

  • Axiom Ref OPHS340

    Class IIb EUDAMEDFDA UDI Active

  • Axiom Ref OPMU18-1-IN

    Class IIb EUDAMEDFDA UDI Active

Showing 301-350 of 837

What Anthogyr Sas makes

Anthogyr Sas makes dental and implantology devices, including motor units, surgical handpieces, and implant systems such as the Anthofit and Axiom lines. Their products include the Implantéo implantology and dental surgical motor unit, and the Montblanc surgical contra-angle and straight handpiece.

The company's portfolio is regulated under Class I and Class II devices and is listed in the FDA 510k registry. Anthogyr Sas is based in the US.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What type of devices does Anthogyr Sas manufacture?

Anthogyr Sas makes dental and implantology devices, including motor units, surgical handpieces, and implant systems, as seen in their product lines such as Anthofit and Axiom.

Where is Anthogyr Sas based?

Anthogyr Sas is based in the US, as indicated by their country listing.

Which regulatory registries list Anthogyr Sas devices?

Anthogyr Sas devices are listed in the FDA 510k registry, which regulates their Class I and Class II devices.

How are Anthogyr Sas devices classified?

Anthogyr Sas devices are classified as either Class I or Class II devices, indicating the level of regulatory control required for their products.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
France(from SRN)
Address
2237, avenue André Lasquin, Sallanches, France
Website
anthogyr.com
PRRC contact
Jérôme DUTHIL
EUDAMED SRN
FR-MF-000000602