Is this your brand? Sign in to claim ownership.

Sign in to claim this brand

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
—
LinkedIn
—
Facebook
—
Email
—
Phone
—
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
340998796

Catalogue (164)

Page 1 of 4
DeviceModel / ReferenceRegistriesClassStatus
OT-F2 / OT-F3 Prosthetics 02-2509001000
FDA UDI
Class IIActive
OT-F2 / OT-F3 Prosthetics 02-2389062610
FDA UDI
Class IIActive
OT-F2 / OT-F3 Prosthetics 02-2419042611
FDA UDI
Class IIActive
OT-F2 Prosthetics 02-4419034510
FDA UDI
Class IIActive
OT-F1 Implant TPS Surface 01-1491120000
FDA UDI
Class IIActive
OT-F1 Implant Nanoplast Surface 01-1382140000
FDA UDI
Class IIActive
OT-F3 Implant 03-1503050010
FDA UDI
Class IIActive
OT-F2 / OT-F3 Prosthetics 02-3419032310
FDA UDI
Class IIActive
OT-F1 Implant TPS Surface 01-1331100000
FDA UDI
Class IIActive
OT-F2 / OT-F3 Prosthetics 02-5419004010
FDA UDI
Class IIActive
OT-F2 / OT-F3 Prosthetics 02-3509032110
FDA UDI
Class IIActive
OT-F2 / OT-F3 Prosthetics 02-3389032310
FDA UDI
Class IIActive
OT-F2 Prosthetics 02-4009004510
FDA UDI
Class IIActive
OT-F2 Implant 02-1502120010
FDA UDI
Class IIActive
OT-F1 Implant TPS Surface 01-1411120000
FDA UDI
Class IIActive
OT-F2 / OT-F3 Prosthetics 02-2419001000
FDA UDI
Class IIActive
OT-F2 / OT-F3 Prosthetics 02-2389042611
FDA UDI
Class IIActive
OT-F1 Implant TPS Surface 01-1381140000
FDA UDI
Class IIActive
OT-F2 / OT-F3 Prosthetics 02-2389022610
FDA UDI
Class IIActive
OT-F2 Implant 02-1382160010
FDA UDI
Class IIActive
OT-F1 Implant Nanoplast Surface 01-1382160000
FDA UDI
Class IIActive
OT-F2 Implant 02-1382100010
FDA UDI
Class IIActive
OT-F2 / OT-F3 Prosthetics 02-5389004010
FDA UDI
Class IIActive
OT-F1 Implant Nanoplast Surface 01-1332100000
FDA UDI
Class IIActive
OT-F1 Implant Nanoplast Surface 01-1492080000
FDA UDI
Class IIActive
OT-F2 / OT-F3 Prosthetics 02-2419005510
FDA UDI
Class IIActive
OT-F2 Implant 02-1342160010
FDA UDI
Class IIActive
OT-F2 / OT-F3 Prosthetics 02-4419022010
FDA UDI
Class IIActive
OT-F1 Prosthetics 01-2499005500
FDA UDI
Class IIActive
OT-F2 / OT-F3 Prosthetics 02-3389042510
FDA UDI
Class IIActive
OT-F1 Implant TPS Surface 01-1491100000
FDA UDI
Class IIActive
OT-F2 Prosthetics 02-4419014310
FDA UDI
Class IIActive
OT-F2 / OT-F3 Prosthetics 02-2509042610
FDA UDI
Class IIActive
InstaFix Shape Memory Fixation System 400-3725
FDA UDI
Class IIActive
OT-F2 Prosthetics 02-4389014110
FDA UDI
Class IIActive
OT-F2 / OT-F3 Prosthetics 02-4419002210
FDA UDI
Class IIActive
OT-F2 Implant 02-1412120010
FDA UDI
Class IIActive
OT-F1 Implant Nanoplast Surface 01-1492120000
FDA UDI
Class IIActive
OT-F2 / OT-F3 Prosthetics 02-4509002210
FDA UDI
Class IIActive
OT-F1 Implant Nanoplast Surface 01-1382100000
FDA UDI
Class IIActive
OT-F1 Implant Nanoplast Surface 01-1412100000
FDA UDI
Class IIActive
OT-F2 / OT-F3 Prosthetics 02-2509062610
FDA UDI
Class IIActive
OT-F1 Prosthetics 01-2499001000
FDA UDI
Class IIActive
OT-F2 / OT-F3 Prosthetics 02-2389001000
FDA UDI
Class IIActive
OT-F2 Implant 02-1342120010
FDA UDI
Class IIActive
OT-F2 Implant 02-1502140010
FDA UDI
Class IIActive
OT-F2 / OT-F3 Prosthetics 02-5509004010
FDA UDI
Class IIActive
OT-F2 / OT-F3 Prosthetics 02-2509005510
FDA UDI
Class IIActive
OT-F1 Implant TPS Surface 01-1331140000
FDA UDI
Class IIActive
OT-F2 Implant 02-1382140010
FDA UDI
Class IIActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

FDA Establishments (1)

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

  • Ot Medical Gmbh Bremen · DE FEI 3008496301