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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 1 of 6
DeviceModel / ReferenceRegistriesClassStatus
Trios® 3 S-Ckit
FDA UDI
Class IIActive
3Shape Scan Bodies DXbox
FDA UDI
Class IActive
3Shape Scan Bodies BI
FDA UDI
Class IActive
Trios® 3 S1-4
FDA UDI
Class IIUnknown
Trios® 3 S2-1
FDA UDI
Class IIUnknown
Trios® T12A-1
FDA UDI
Class IIUnknown
3Shape Scan Bodies CC
FDA UDI
Class IActive
Trios® P13-Ckit
FDA UDI
Class IIActive
Trios® 3 S1P-2
FDA UDI
Class IIUnknown
Trios® 3 S1A-4
FDA UDI
Class IIUnknown
3Shape Scan Bodies NCbox
FDA UDI
Class IUnknown
Trios® 4 TST-03
FDA UDI
Class IIActive
3Shape Scan Bodies NRbox
FDA UDI
Class IUnknown
Trios TRIOS Color scanner
FDA UDI
Class IIUnknown
Trios TRIOS Pod
FDA UDI
Class IIUnknown
Trios® 3 S1P-1
FDA UDI
Class IIUnknown
Trios LP1-2
FDA UDI
Class IIActive
3Shape Scan Bodies ZTY
FDA UDI
Class IActive
3Shape Scan Bodies DYbox
FDA UDI
Class IUnknown
Trios® C3B
FDA UDI
Class IIUnknown
TRIOS Patient Monitoring 2.1.4
FDA UDI
Class IIUnknown
Trios 5 L1P-1F
FDA UDI
Class IIActive
3Shape Scan Bodies NB
FDA UDI
Class IActive
Trios® 3 S2A-10
FDA UDI
Class IIUnknown
3Shape Scan Bodies NCY
FDA UDI
Class IActive
Trios C2BP
FDA UDI
Class IIActive
Trios TRIOS Calibration Tip
FDA UDI
Class IIUnknown
Trios® TB-031
FDA UDI
Class IIActive
Trios 3 TRIOS 3 Color Calibration Kit
FDA UDI
Class IIUnknown
TRIOS Ready Tip TST-15
FDA UDI
Class IIActive
3Shape Scan Bodies NCB
FDA UDI
Class IActive
Trios® T12P-1
FDA UDI
Class IIUnknown
3Shape Scan Bodies BCG
FDA UDI
Class IActive
3Shape Scan Bodies NAW
FDA UDI
Class IActive
Trios 3 TRIOS 3 Handle scanner
FDA UDI
Class IIUnknown
3Shape Scan Bodies SSsys
FDA UDI
Class IIActive
Trios® 3 S2A-18
FDA UDI
Class IIActive
3Shape Scan Bodies BEG
FDA UDI
Class IActive
3Shape A47.B
FDA UDI
Class IIUnknown
Trios® 3 S-Ckit-3DD
FDA UDI
Class IIActive
Trios TRIOS Color Scanner Tip
FDA UDI
Class IIUnknown
PrograScan One+ S3-2
FDA UDI
Class IIUnknown
3Shape Scan Bodies ZTG
FDA UDI
Class IActive
3Shape Scan Bodies DAS
FDA UDI
Class IActive
Trios 3 S1P-2
FDA UDI
Class IIActive
Trios® C4.1
FDA UDI
Class IIActive
3Shape Scan Bodies OTbox
FDA UDI
Class IUnknown
PrograScan One S1-2
FDA UDI
Class IIUnknown
3Shape Scan Bodies NR
FDA UDI
Class IActive
3Shape Scan Bodies BE
FDA UDI
Class IActive

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