Telio Cad

by Ivoclar Vivadent, Inc.

510(k) K093708

Telio Cad is a Class II device made by Ivoclar Vivadent, Inc., cleared under FDA 510(k) K093708 on 10 Mar 2010, active as of 22 Oct 2026.

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

510(k) K093708↗

FDA record

Trust

Source FDA 510(k), synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	FDA 510(k)SESE Substantially Equivalent · Traditional	NumberK093708	Date10 Mar 2010Cleared	StatusActive

Official records

FDA 510(k) database 510(k) number K093708

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number: K093708
FDA product code: EBG

Device class: Class II
Regulation: 21 CFR Part 872.3770
Advisory committee: Dental
FDA decision: SESE Substantially Equivalent

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