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3shape Trios A/S

US

Last updated May 24, 2026

What 3shape Trios A/S makes

3shape Trios A/S manufactures intraoral optical scanning systems for capturing digital impressions of dental structures, as well as CAD/CAM dental milling systems designed for both laboratory and chairside use. Their portfolio includes devices for intraoral scanning and scan bodies used in restorative dentistry workflows, enabling precise digital records for crowns, bridges, and other dental prosthetics.

The company’s devices are regulated under FDA classifications, including Class I and Class II, and are listed under the 510(k) and UDI programs. Their products are based in the United States and comply with applicable regulatory requirements for dental imaging and milling systems.

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 Trios A/S manufacture?

3shape Trios A/S specializes in dental devices, including intraoral optical scanning systems for capturing digital impressions of teeth and gums, as well as CAD/CAM dental milling systems. These systems are used in both laboratory and chairside settings to create precise digital records for dental restorations like crowns, bridges, and other prosthetics. Their portfolio also includes scan bodies, which are used in conjunction with intraoral scanners to aid in the fabrication of dental restorations.

Where is 3shape Trios A/S based, and how does this affect its regulatory oversight?

3shape Trios A/S is based in the United States, which means its devices fall under FDA regulatory jurisdiction. The company’s products are classified under FDA categories, including Class I (generally low-risk devices) and Class II (devices requiring special controls to ensure safety and effectiveness). This classification determines the regulatory pathway, such as the 510(k) premarket notification process or UDI (Unique Device Identification) requirements, ensuring compliance with U.S. medical device regulations.

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

3shape Trios A/S devices are listed in the FDA’s 510(k) database, which tracks premarket submissions for Class II devices requiring special controls, and the FDA’s UDI (Unique Device Identification) system. These registries help ensure transparency and traceability of the company’s products under U.S. medical device regulations. Listing in these databases confirms compliance with FDA requirements for device identification and classification.

How are 3shape Trios A/S devices classified under FDA regulations?

3shape Trios A/S devices are classified under FDA’s risk-based system as either Class I or Class II. Class I devices, such as some intraoral scanners, are typically low-risk and may only require general controls like good manufacturing practices. Class II devices, including certain CAD/CAM milling systems, require additional regulatory oversight, such as the 510(k) process, to ensure their safety and performance meet FDA standards. Classification depends on factors like intended use, risk level, and technological complexity.

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
305225025

Catalogue (256)

Page 3 of 6
DeviceModel / ReferenceRegistriesClassStatus
Trios 3 TRIOS 3 Calibration Tip
FDA UDI
Class IIUnknown
3Shape Scan Bodies ZTsys
FDA UDI
Class IActive
Trios® T12-Ctip
FDA UDI
Class IIActive
Trios® 4 S3A-10
FDA UDI
Class IIUnknown
3Shape Scan Bodies SSR
FDA UDI
Class IActive
3Shape Scan Bodies CCbox
FDA UDI
Class IUnknown
Trios® 3 S2P-1
FDA UDI
Class IIUnknown
3Shape Scan Bodies DEG
FDA UDI
Class IActive
Trios® 4 TSC-01
FDA UDI
Class IIActive
3Shape Scan Bodies DXB
FDA UDI
Class IActive
Trios 3 TRIOS 3 Pod for pen grip
FDA UDI
Class IIUnknown
Trios TRIOS Color Calibration Kit
FDA UDI
Class IIUnknown
Trios® 3 S1A-2
FDA UDI
Class IIUnknown
Trios® 4 PS3-4
FDA UDI
Class IIActive
3Shape Scan Bodies SSbox
FDA UDI
Class IUnknown
Trios® 3 S-Ctip
FDA UDI
Class IIActive
Trios® 4 S3A-18
FDA UDI
Class IIActive
Trios® 3 S2A-2
FDA UDI
Class IIUnknown
3Shape Scan Bodies BEY
FDA UDI
Class IActive
3Shape Scan Bodies OT
FDA UDI
Class IActive
3Shape Scan Bodies ZTbox
FDA UDI
Class IUnknown
Trios® 3 S2A-5
FDA UDI
Class IIUnknown
Trios 3 PS1-2
FDA UDI
Class IIActive
3Shape Scan Bodies CCY
FDA UDI
Class IActive
3Shape Scan Bodies DE5
FDA UDI
Class IActive
Trios® T12A-2
FDA UDI
Class IIUnknown
3Shape Scan Bodies NRDsys
FDA UDI
Class IActive
Trios® P12-tip
FDA UDI
Class IIActive
3Shape Scan Bodies NAN
FDA UDI
Class IActive
3Shape Scan Bodies NBR
FDA UDI
Class IActive
Trios® C3BP
FDA UDI
Class IIActive
3Shape Scan Bodies DAbox
FDA UDI
Class IUnknown
Trios® 3 PS2-2
FDA UDI
Class IIActive
Trios 3 TRIOS 3 Protection Tip
FDA UDI
Class IIUnknown
3Shape Scan Bodies NRN
FDA UDI
Class IActive
3Shape Scan Bodies NGbox
FDA UDI
Class IUnknown
3Shape Scan Bodies DX3
FDA UDI
Class IActive
3Shape Scan Bodies NA
FDA UDI
Class IActive
3Shape Scan Bodies BIG
FDA UDI
Class IActive
3Shape Scan Bodies BCB
FDA UDI
Class IActive
Trios® 3 S2-2
FDA UDI
Class IIActive
Trios® 3 PS1-2
FDA UDI
Class IIUnknown
Trios® 3 S2A-17
FDA UDI
Class IIUnknown
Trios® 3 S1A-11
FDA UDI
Class IIUnknown
3Shape Scan Bodies NCP
FDA UDI
Class IActive
3Shape Scan Bodies NBbox
FDA UDI
Class IUnknown
Trios® C4.0
FDA UDI
Class IIUnknown
Trios® 3 PS2-1
FDA UDI
Class IIActive
3Shape Scan Bodies DAX
FDA UDI
Class IActive
3Shape Scan Bodies DYG
FDA UDI
Class IActive

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