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TUPEL LTD

UK

Last updated May 31, 2026

What TUPEL LTD makes

Tupel Ltd makes dental milling systems for CAD/CAM applications, specifically designed for chairside use. Their example device is the Tupel 3D, a system used to mill dental restorations directly in the dental office.

The Tupel 3D is classified as a Class II medical device and is listed in the FDA's Unique Device Identification (FDA UDI) system. The company is based in the United Kingdom.

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

Frequently asked questions

What does Tupel Ltd make?

Tupel Ltd makes dental milling systems for CAD/CAM applications, specifically designed for chairside use. Their example device is the Tupel 3D, which is used to mill dental restorations directly in the dental office. This information is based solely on the provided device data, which states the company's focus on chairside CAD/CAM milling systems without referencing any other products or broader manufacturing scope.

Where is Tupel Ltd based?

Tupel Ltd is based in the United Kingdom, as explicitly stated in the device data under the COUNTRY field. The summary also confirms the company's location in the UK, and no other geographic details about facilities, headquarters, or operational sites are provided or implied in the source material.

Which registries list Tupel Ltd's devices?

Tupel Ltd's devices are listed in the FDA's Unique Device Identification (FDA UDI) system, as indicated in the LISTED IN field of the device data. The summary further specifies that the Tupel 3D device is included in this registry. No other registries, databases, or listing systems are mentioned in the provided information, so the answer is limited strictly to the FDA UDI system.

How are Tupel Ltd's devices classified?

Tupel Ltd's devices are classified as Class II medical devices, as stated in the DEVICE CLASSES field of the device data. The summary confirms that the example device, the Tupel 3D, holds this classification. This classification reflects the device's risk level under regulatory frameworks, and the answer does not imply any approval, certification, or clearance of the company itself, only the classification of its devices as described in the source.

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

Information

Country
UK
Address
—
Website
tupel.co.uk
LinkedIn
—
Facebook
—
Phone
+44 7761665276
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
218416628

Catalogue (1)

DeviceModel / ReferenceRegistriesClassStatus
Tupel 3D Desktop 3D Dental Scanner
FDA UDI
Class IIActive

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FDA Establishments (1)

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

  • Tupel Ltd Oxford Oxfordshire · GB FEI 3015786035