FDA device listing

TrueDent Clear,TrueDent Cyan,TrueDent Magenta,TrueDent White,TrueDent Yellow

FDA device listing 1990994584 · Stratasys Ltd

Key facts

Proprietary names TrueDent Clear,TrueDent Cyan,TrueDent Magenta,TrueDent White,TrueDent Yellow
Owner/operator Stratasys Ltd
Owner/operator number 10086646
Premarket submissions K220771
Product codes EBF, EBG, EBI, PZY
Device names EBF - Material, Tooth Shade, Resin, EBG - Crown And Bridge, Temporary, Resin, EBI - Resin, Denture, Relining, Repairing, Rebasing, PZY - Additively Manufactured, Preformed, Resin Denture Tooth
Device class Class II
Classification regulations (21 CFR) 872.3590, 872.3690, 872.3760, 872.3770
Review panels Dental
Registered establishments STRATASYS LTD, STRATASYS LTD - Headquarter
Establishment registrations 3016074824, 3017374693
FEI numbers 3016074824, 3017374693
Establishment operations Complaint File Establishment, Specification Developer, Manufacturer
Registration valid through 2026

At a glance

  • 1–9 Registered establishments listing this device
  • 1–9 UDI devices (GUDID) under the same submission
  • 1–9 Device listings citing the same submission
  • Yes Premarket submission listed

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA device listings

Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.

Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database

Browse all FDA device listings