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3shape A/S

US

Last updated May 24, 2026

What 3shape A/S makes

3shape A/S develops dental milling systems and CAD/CAM software tailored for laboratory use, including devices for scanning dental models and designing restorations such as abutments and splints. Their portfolio also includes specialized software applications for dental treatment planning, including orthodontic workflows and implant design tools.

The company’s devices are classified under Class II and Class U, with regulatory authorisation through FDA 510(k) clearances and FDA UDI listings. These products are intended for use in the United States, where the manufacturer is based.

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 3shape A/S manufacture?

3shape A/S specializes in dental devices primarily used in laboratory settings. Their portfolio includes CAD/CAM milling systems for creating dental restorations, as well as software applications for designing dental treatments. Examples include devices for scanning dental models (Lab Scanner), designing abutments and splints (Abutment Design, Splint Design), and specialized software for orthodontic workflows (Ortho System) and implant planning (Implant Studio). These tools are designed to streamline workflows for dental laboratories and clinicians.

Where is 3shape A/S based, and what is its primary market?

3shape A/S is based in the United States. While the company develops its devices globally, its primary market focus is the U.S., where its products are intended for use. The devices are tailored to meet regulatory requirements and workflows specific to this market.

How are 3shape A/S’s devices classified under U.S. regulations?

3shape A/S’s devices fall under two primary regulatory classifications in the U.S.: Class II and Class U. Class II devices generally require premarket notification (510(k)) clearance to demonstrate substantial equivalence to a predicate device, while Class U devices are exempt from certain regulatory requirements but still must comply with UDI (Unique Device Identification) rules. The company’s portfolio includes both types, depending on the specific function and risk level of the device.

Which regulatory registries or databases list 3shape A/S’s devices?

3shape A/S’s devices are listed in the FDA’s 510(k) database for Class II devices, which requires premarket notification clearance. Additionally, their devices appear in the FDA’s UDI (Unique Device Identification) system, ensuring traceability and compliance with identification requirements. These listings help ensure transparency and accessibility for regulatory oversight and market surveillance.

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

Information

Country
US
Address
—
Website
3shape.com
LinkedIn
—
Facebook
—
Phone
+4570272620
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
306826012

Catalogue (175)

Page 1 of 4
DeviceModel / ReferenceRegistriesClassStatus
Lab Scanner D750
FDA UDI
Class IIUnknown
Lab Scanner A45.II
FDA UDI
Class IIUnknown
Lab Scanner A38.II
FDA UDI
Class IIUnknown
3Shape scan bodies NGG
FDA UDI
Class IIUnknown
Lab Scanner F27
FDA UDI
Class IIUnknown
Puffin R1.0
FDA UDI
Class IIUnknown
3Shape Scan Posts CL1.40
FDA UDI
Class IIUnknown
3Shape Anatomy Design 2016-1
FDA UDI
Class IIUnknown
3Shape Scan Posts PIVsys
FDA UDI
Class IIUnknown
Lab Scanner A32
FDA UDI
Class IIUnknown
3Shape Scan Posts PIVbox
FDA UDI
Class IIUnknown
3Shape scan bodies NC5
FDA UDI
Class IIUnknown
Ortho System 2017-1
FDA UDI
Class IIUnknown
Lab Scanner E3N
FDA UDI
Class IIActive
3Shape D700
FDA UDI
Class IIUnknown
Dental System 2017-1
FDA UDI
Class IIUnknown
Lab Scanner R850
FDA UDI
Class IIUnknown
3Shape scan bodies NCbox
FDA UDI
Class IIUnknown
3Shape Scan Bodies DYsys
FDA UDI
Class IIUnknown
Lab Scanner A45.I
FDA UDI
Class IIUnknown
Lab Scanner A39.IP
FDA UDI
Class IIUnknown
Abutment Design 2017-1 (R1.1)
FDA UDI
Class IIActive
Ortho System 2018-1
FDA UDI
Class IIUnknown
Implant Studio R1.4
FDA UDI
Class IIActive
Dental System 2018-1
FDA UDI
Class IIUnknown
Lab Scanner A49.II
FDA UDI
Class IIUnknown
Splint Design R1.0
FDA UDI
Class IIActive
3Shape Scan Posts AS1.6
FDA UDI
Class IIUnknown
3Shape scan bodies NCB
FDA UDI
Class IIUnknown
Automate R1.3
FDA UDI
Class IIActive
3Shape D900L
FDA UDI
Class IIUnknown
3Shape R750
FDA UDI
Class IIUnknown
Lab Scanner A22
FDA UDI
Class IUnknown
Lab Scanner D900
FDA UDI
Class IIUnknown
Lab Scanner R900
FDA UDI
Class IIUnknown
3Shape Scan Posts CS1.40
FDA UDI
Class IIUnknown
3Shape Scan Posts CS1.14
FDA UDI
Class IIUnknown
Lab Scanner D750N
FDA UDI
Class IIUnknown
3Shape Scan Bodies NBsys
FDA UDI
Class IIUnknown
3Shape Scan Posts CL1.14
FDA UDI
Class IIUnknown
Lab Scanner E2N
FDA UDI
Class IIActive
Lab Scanner D500
FDA UDI
Class IIUnknown
3Shape Scan Posts CL1.50
FDA UDI
Class IIUnknown
Lab Scanner D810
FDA UDI
Class IIUnknown
3Shape Scan Posts CYLbox
FDA UDI
Class IIUnknown
3Shape Ortho System 2015-1
FDA UDI
Class IIUnknown
Lab Scanner R900L
FDA UDI
Class IIUnknown
Lab Scanner R750
FDA UDI
Class IIUnknown
Ortho System 85.x
FDA UDI
Class IIActive
3Shape Scan Bodies NRDsys
FDA UDI
Class IIUnknown

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