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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
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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 3 of 4
DeviceModel / ReferenceRegistriesClassStatus
OT-F1 Prosthetics 01-2389022600
FDA UDI
Class IIActive
OT-F2 Prosthetics 02-4419034310
FDA UDI
Class IIActive
OT-F1 Implant Nanoplast Surface 01-1382120000
FDA UDI
Class IIActive
OT-F2 Prosthetics 02-4419034110
FDA UDI
Class IIActive
OT-F1 Prosthetics 01-2419001000
FDA UDI
Class IIActive
OT-F3 Implant 03-1383070010
FDA UDI
Class IIActive
InstaFix Shape Memory Fixation System 400-3701
FDA UDI
Class IIActive
OT-F2 / OT-F3 Prosthetics 02-4419042010
FDA UDI
Class IIActive
OT-F2 / OT-F3 Prosthetics 02-4509041010
FDA UDI
Class IIActive
OT-F2 / OT-F3 Prosthetics 02-3509012510
FDA UDI
Class IIActive
OT-F2 Implant 02-1342100010
FDA UDI
Class IIActive
OT-F2 / OT-F3 Prosthetics 02-3509032310
FDA UDI
Class IIActive
OT-F2 / OT-F3 Prosthetics 02-4419041010
FDA UDI
Class IIActive
InstaFix Shape Memory Fixation System 400-3723
FDA UDI
Class IIActive
OT-F1 Implant Nanoplast Surface 01-1492100000
FDA UDI
Class IIActive
InstaFix Shape Memory Fixation System 400-3724
FDA UDI
Class IIActive
OT-F1 Implant TPS Surface 01-1331080000
FDA UDI
Class IIActive
OT-F2 / OT-F3 Prosthetics 02-2419062611
FDA UDI
Class IIActive
OT-F2 / OT-F3 Prosthetics 02-2509042611
FDA UDI
Class IIActive
OT-F1 Implant TPS Surface 01-1381120000
FDA UDI
Class IIActive
OT-F2 / OT-F3 Prosthetics 02-4389042010
FDA UDI
Class IIActive
OT-F3 Implant 03-1503090010
FDA UDI
Class IIActive
OT-F2 Prosthetics 02-4009004110
FDA UDI
Class IIActive
OT-F2 / OT-F3 Prosthetics 02-4509022010
FDA UDI
Class IIActive
OT-F2 / OT-F3 Prosthetics 02-4419021010
FDA UDI
Class IIActive
OT-F1 Implant Nanoplast Surface 01-1412080000
FDA UDI
Class IIActive
OT-F2 / OT-F3 Prosthetics 02-8419104000
FDA UDI
Class IIActive
OT-F2 / OT-F3 Prosthetics 02-3509042510
FDA UDI
Class IIActive
OT-F2 / OT-F3 Prosthetics 02-8389104000
FDA UDI
Class IIActive
OT-F2 Prosthetics 02-4419014110
FDA UDI
Class IIActive
OT-F2 Implant 02-1502080010
FDA UDI
Class IIActive
OT-F2 Implant 02-1412160010
FDA UDI
Class IIActive
OT-F2 / OT-F3 Prosthetics 02-2389042610
FDA UDI
Class IIActive
OT-F1 Implant Nanoplast Surface 01-1412120000
FDA UDI
Class IIActive
OT-F1 Implant TPS Surface 01-1331120000
FDA UDI
Class IIActive
OT-F3 Implant 03-1413090010
FDA UDI
Class IIActive
OT-F2 Prosthetics 02-4419014510
FDA UDI
Class IIActive
OT-F2 Prosthetics 02-8149054000
FDA UDI
Class IIActive
OT-F1 Implant TPS Surface 01-1411140000
FDA UDI
Class IIActive
OT-F1 Implant TPS Surface 01-1491140000
FDA UDI
Class IIActive
OT-F1 Prosthetics 01-2339005500
FDA UDI
Class IIActive
OT-F2 Implant 02-1412080010
FDA UDI
Class IIActive
OT-F1 Implant Nanoplast Surface 01-1412160000
FDA UDI
Class IIActive
OT-F1 Implant TPS Surface 01-1411080000
FDA UDI
Class IIActive
OT-F1 Prosthetics 01-2389005500
FDA UDI
Class IIActive
InstaFix Shape Memory Fixation System 400-3722
FDA UDI
Class IIActive
OT-F3 Implant 03-1413050010
FDA UDI
Class IIActive
OT-F2 / OT-F3 Prosthetics 02-4389022010
FDA UDI
Class IIActive
OT-F1 Implant Nanoplast Surface 01-1382080000
FDA UDI
Class IIActive
OT-F2 Implant 02-1502100010
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