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OT medical GmbH

US

Last updated May 23, 2026

What OT medical GmbH makes

OT medical GmbH manufactures one-piece screw endosteal dental implants and non-adjustable orthopaedic bone staples. Their portfolio includes implant surfaces (TPS and Nanoplast) and prosthetic systems (OT-F1, OT-F2, OT-F3) designed for dental and orthopaedic applications.

The company’s devices are classified as Class II under FDA regulations and are listed via 510(k) and UDI pathways. Their products are registered in the United States.

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 OT medical GmbH manufacture?

OT medical GmbH specializes in two primary device categories: screw endosteal dental implants (one-piece) and non-adjustable orthopaedic bone staples. Their portfolio also includes dental implant surfaces (such as TPS and Nanoplast) and prosthetic systems (e.g., OT-F1, OT-F2, OT-F3) tailored for dental and orthopaedic applications. These devices are designed to support bone integration and structural stability in respective medical fields.

Where is OT medical GmbH based, and where are their devices registered?

OT medical GmbH is based in the United States. Their devices are registered and listed in the U.S. regulatory system, specifically through the FDA’s 510(k) and UDI (Unique Device Identification) pathways. This ensures compliance with U.S. medical device regulations.

How are OT medical GmbH’s devices classified under FDA regulations?

All of OT medical GmbH’s devices fall under Class II classification according to FDA regulations. This classification applies to devices that generally pose moderate risk and require special controls to ensure safety and effectiveness, such as dental implants and orthopaedic staples.

Which regulatory registries or databases list OT medical GmbH’s devices?

OT medical GmbH’s devices are listed in the FDA’s 510(k) database and the FDA’s UDI (Unique Device Identification) system. These registries track device submissions, clearances, and compliance with U.S. regulatory requirements, ensuring transparency and traceability for healthcare providers and regulators.

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

Information

Country
US
Address
—
Website
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LinkedIn
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Facebook
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Email
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Phone
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PRRC Contact
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EUDAMED SRN
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FDA FEI Number
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DUNS Number
340998796

Catalogue (164)

Page 2 of 4
DeviceModel / ReferenceRegistriesClassStatus
OT-F2 Implant 02-1342140010
FDA UDI
Class IIActive
OT-F1 Implant Nanoplast Surface 01-1332140000
FDA UDI
Class IIActive
OT-F2 Prosthetics 02-4389014510
FDA UDI
Class IIActive
OT-F2 / OT-F3 Prosthetics 02-2389042710
FDA UDI
Class IIActive
OT-F2 Prosthetics 02-4389034110
FDA UDI
Class IIActive
InstaFix Shape Memory Fixation System 400-3715
FDA UDI
Class IIActive
OT-F2 / OT-F3 Prosthetics 02-8509104000
FDA UDI
Class IIActive
OT-F2 / OT-F3 Prosthetics 02-2509062611
FDA UDI
Class IIActive
OT-F1 Prosthetics 01-2339022600
FDA UDI
Class IIActive
OT-F1 Implant TPS Surface 01-1381160000
FDA UDI
Class IIActive
OT-F2 / OT-F3 Prosthetics 02-3389032110
FDA UDI
Class IIActive
OT-F1 Implant TPS Surface 01-1411160000
FDA UDI
Class IIActive
OT-F2 / OT-F3 Prosthetics 02-4389002210
FDA UDI
Class IIActive
OT-F2 / OT-F3 Prosthetics 02-4509042010
FDA UDI
Class IIActive
OT-F2 Prosthetics 02-4389034510
FDA UDI
Class IIActive
InstaFix Shape Memory Fixation System 400-3721
FDA UDI
Class IIActive
OT-F2 / OT-F3 Prosthetics 02-3419042510
FDA UDI
Class IIActive
OT-F2 / OT-F3 Prosthetics 02-3389012310
FDA UDI
Class IIActive
OT-F1 Implant TPS Surface 01-1381100000
FDA UDI
Class IIActive
OT-F2 / OT-F3 Prosthetics 02-4509021010
FDA UDI
Class IIActive
InstaFix Shape Memory Fixation System 400-3703
FDA UDI
Class IIActive
OT-F2 Implant 02-1382080010
FDA UDI
Class IIActive
OT-F1 Implant TPS Surface 01-1381080000
FDA UDI
Class IIActive
OT-F2 Implant 02-1382120010
FDA UDI
Class IIActive
OT-F2 / OT-F3 Prosthetics 02-3419012110
FDA UDI
Class IIActive
OT-F1 Implant Nanoplast Surface 01-1332080000
FDA UDI
Class IIActive
OT-F2 / OT-F3 Prosthetics 02-3419032110
FDA UDI
Class IIActive
OT-F1 Implant Nanoplast Surface 01-1492140000
FDA UDI
Class IIActive
OT-F1 Implant TPS Surface 01-1411100000
FDA UDI
Class IIActive
OT-F2 / OT-F3 Prosthetics 02-3419012310
FDA UDI
Class IIActive
OT-F2 / OT-F3 Prosthetics 02-2389005510
FDA UDI
Class IIActive
OT-F1 Implant Nanoplast Surface 01-1412140000
FDA UDI
Class IIActive
OT-F1 Implant Nanoplast Surface 01-1332160000
FDA UDI
Class IIActive
OT-F2 / OT-F3 Prosthetics 02-2509042710
FDA UDI
Class IIActive
OT-F2 Implant 02-1412100010
FDA UDI
Class IIActive
OT-F1 Prosthetics 01-2389001000
FDA UDI
Class IIActive
OT-F2 / OT-F3 Prosthetics 02-2509022610
FDA UDI
Class IIActive
OT-F2 / OT-F3 Prosthetics 02-3389012510
FDA UDI
Class IIActive
OT-F2 / OT-F3 Prosthetics 02-3419012510
FDA UDI
Class IIActive
OT-F2 / OT-F3 Prosthetics 02-2389062611
FDA UDI
Class IIActive
OT-F2 Implant 02-1412140010
FDA UDI
Class IIActive
OT-F2 / OT-F3 Prosthetics 02-3389012110
FDA UDI
Class IIActive
OT-F3 Implant 03-1503070010
FDA UDI
Class IIActive
OT-F2 / OT-F3 Prosthetics 02-2419022610
FDA UDI
Class IIActive
OT-F2 Implant 02-1342080010
FDA UDI
Class IIActive
OT-F2 / OT-F3 Prosthetics 02-2419042710
FDA UDI
Class IIActive
OT-F1 Implant TPS Surface 01-1491080000
FDA UDI
Class IIActive
OT-F1 Prosthetics 01-2339001000
FDA UDI
Class IIActive
OT-F2 / OT-F3 Prosthetics 02-3509012310
FDA UDI
Class IIActive
OT-F2 / OT-F3 Prosthetics 02-3509012110
FDA UDI
Class IIActive

Related Companies

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FDA Establishments (1)

Establishments registered with the FDA under this company group, matched by name.

  • Ot Medical Gmbh Bremen · DE FEI 3008496301