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ETABLISSEMENTS ANTHOGYR

US

Last updated May 24, 2026

What ETABLISSEMENTS ANTHOGYR makes

The company manufactures reusable and single-use dental implant suprastructures, including temporary and permanent preformed types, as well as dental implant abutment analogs designed for laboratory use. Their portfolio also includes reusable dental drill bits, surgical screwdrivers, depth limiters for implants, and reusable bone taps, all tailored for dental and surgical procedures.

These devices are classified under FDA regulations as Class I and Class II, with listings maintained in the FDA’s Unique Device Identifier (UDI) database. The company operates from the United States, adhering to applicable regulatory standards for medical devices in that jurisdiction.

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

Frequently asked questions

What types of medical devices does Etablissements Anthogyr manufacture?

Etablissements Anthogyr specializes in dental and surgical devices. Their portfolio includes reusable and single-use dental implant suprastructures (both temporary and permanent preformed types), dental implant abutment analogs for laboratory use, dental drill bits, surgical screwdrivers, depth limiters for implants, and reusable bone taps. These devices are designed for precision in dental and surgical procedures.

Where is Etablissements Anthogyr based?

Etablissements Anthogyr is based in the United States. The company operates within this jurisdiction, ensuring its devices comply with applicable U.S. regulatory standards for medical devices.

Which regulatory registries list Etablissements Anthogyr’s devices?

Etablissements Anthogyr’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify their products under FDA regulations, ensuring transparency and traceability for authorized devices.

How are Etablissements Anthogyr’s devices classified under FDA regulations?

Etablissements Anthogyr’s devices fall under two FDA classification categories: Class I and Class II. Class I devices generally pose minimal risk and may require general controls, while Class II devices involve a higher level of risk and may require special controls to ensure safety and effectiveness. The classification depends on the specific device type and its intended use.

What distinguishes Etablissements Anthogyr’s dental implant suprastructures from other similar devices?

Etablissements Anthogyr offers both reusable and single-use dental implant suprastructures, including temporary and permanent preformed types. The distinction lies in their design for specific procedural needs—temporary suprastructures may be used for interim support, while permanent ones provide long-term stability. The company’s portfolio also includes reusable alternatives, catering to practices prioritizing cost efficiency and sustainability.

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

Information

Country
US
Address
—
Website
anthogyr.com
LinkedIn
—
Facebook
—
Phone
+33450584888
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
275978864

Catalogue (274)

Page 1 of 6
DeviceModel / ReferenceRegistriesClassStatus
Axiom® OPAF02-7
FDA UDI
Class IActive
Axiom OPSC010
FDA UDI
Class IIActive
Axiom® 151-04-PA
FDA UDI
Class IActive
Axiom® OPB4806L
FDA UDI
Class IActive
Axiom PX34080
FDA UDI
Class IIActive
Axiom OPFS100
FDA UDI
Class IIActive
Axiom® GFE30L8G36
FDA UDI
Class IActive
Axiom® OPAF032
FDA UDI
Class IActive
Axiom® 152-27-PA
FDA UDI
Class IActive
Axiom OPAC140
FDA UDI
Class IIActive
Axiom® OPROFIL410
FDA UDI
Class IActive
Axiom® INCCDC
FDA UDI
Class IActive
Axiom® INPIL
FDA UDI
Class IActive
Axiom® GTIMG50S
FDA UDI
Class IActive
Axiom® OPB3006L
FDA UDI
Class IActive
Axiom® OPPU102L
FDA UDI
Class IActive
Axiom® INBW100XL
FDA UDI
Class IActive
Axiom® OPFLEX413-ET
FDA UDI
Class IIActive
Axiom® 151-03-PA
FDA UDI
Class IActive
Axiom OPLA030
FDA UDI
Class IIActive
Axiom OPAT212
FDA UDI
Class IIActive
Axiom® GFI20L10G50
FDA UDI
Class IActive
Axiom® PROSTHSET-WS
FDA UDI
Class IActive
Axiom® MUNT200-4
FDA UDI
Class IActive
Axiom® XT40100
FDA UDI
Class IIActive
Axiom® GFE24L8G50
FDA UDI
Class IActive
Axiom® MUFLEX
FDA UDI
Class IIActive
Axiom OPSC800
FDA UDI
Class IIActive
Axiom® GFI20L8G42
FDA UDI
Class IActive
Axiom® GFE36L12G42
FDA UDI
Class IActive
Axiom® GPDG42L
FDA UDI
Class IActive
Axiom® OPGS20-ET
EUDAMEDFDA UDI
Class IActive
Axiom OPHS630
FDA UDI
Class IIActive
Axiom® GFI20L6G36
FDA UDI
Class IActive
Axiom® GFE24L12G36
FDA UDI
Class IActive
Axiom OPACR43
FDA UDI
Class IIActive
Axiom® GFE36L14G42
FDA UDI
Class IActive
Axiom® GFE42L14G50
FDA UDI
Class IActive
Axiom® OPGS42
FDA UDI
Class IActive
Axiom® GFI20L6G42
FDA UDI
Class IActive
Axiom OPAC042
FDA UDI
Class IIActive
Axiom® GFE30L12G36
FDA UDI
Class IActive
Axiom® GTA40G42S
FDA UDI
Class IActive
Anthogyr OSTEOTOME EXO_FULLS
FDA UDI
Class IActive
Axiom® INCCD
FDA UDI
Class IActive
Axiom® 152-27-PA-ET
FDA UDI
Class IActive
Axiom® OPGS42-ET
FDA UDI
Class IActive
Axiom® INBM100S
FDA UDI
Class IActive
Axiom® INCHECV
FDA UDI
Class IActive
Axiom OPTP500
FDA UDI
Class IIActive

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