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Dentca, Inc.

Active in EUDAMED

United Statesfrom SRN EUDAMED FDA SRN US-MF-000007372 FEI 3009312537

Dentca, Inc. is a medical device manufacturer based in the United States, with 79 devices listed in FDA GUDID, FDA 510(k) and EUDAMED (FDA Class II and I) as of 15 Nov 2026.

Devices
79
Registrations
EUDAMEDFDA
FDA recalls
0

Registry facts

Counted by deviCERTS from registry records, 15 Nov 2026

Registries
  • FDA GUDID 74
  • FDA 510(k) 6
  • EUDAMED 5

A device listed in two registries counts in both.

Device classes
  • FDA Class II 69
  • FDA Class I 10
Identifiers
  • EUDAMED SRN US-MF-000007372
  • FDA FEI 3009312537
  • DUNS 022455143

At a glance

Counted by deviCERTS from registry records

Market reach

European Union
EUDAMED actor
United States
FDA FEI

What Dentca, Inc. makes

Dentca, Inc. makes dental appliance fabrication materials including resins for denture teeth, temporary crowns and bridges, and single-use impression trays. They also produce CAD/CAM software and specific products such as Dentca Denture Teeth for Carbon Printers, Dentca Tray, Dentca Crown and Bridge, and Formlabs Denture Teeth and Base resins.

The company's devices are classified as Class I and Class II medical devices and are listed in the FDA 510(k) and FDA UDI registries. Dentca, Inc. is based in the United States.

AI-generated from registry data, 4 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue79

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Company details

EUDAMED record synced 7 Nov 2026

EUDAMED SRN
US-MF-000007372
FDA FEI number
3009312537
DUNS number
022455143
EUDAMED status
Active
EUDAMED registered name
DENTCA, Inc.
Registered address
17742 Cowan, CA 92614, Irvine, United States
Phone
+1(424)558-8726
PRRC contact
JASON LEE(public in EUDAMED)

Frequently asked questions

How many devices does DENTCA, INC. have in the registry?

The registry currently lists 79 devices for DENTCA, INC.. Devices recorded under merged duplicate company entries are counted once.

Which registries list DENTCA, INC.'s devices?

Among its 50 most recently registered devices, DENTCA, INC. has devices listed in EUDAMED (4 devices), FDA 510(k) (1 device) and FDA GUDID (49 devices). A device can be listed in more than one registry, so these counts overlap.

What risk classes do DENTCA, INC.'s devices fall under?

Among its 50 most recently registered devices, the classes recorded for DENTCA, INC.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from DENTCA, INC. in the registry?

The most recently registered devices listed for DENTCA, INC. include DENTCA Tru Flexible, DENTCA Denture Teeth for Carbon Printers, DENTCA Tray Single Arch Attachment(U&L)-S&M and DENTCA Crown and Bridge.

Generated automatically from registry data and not verified by a human reviewer.