Trilor Disks, Blocks and Arches

FDA 510(k) K173643 · Bioloren S.R.L.

Substantially Equivalent

510(k) numberK173643

Submission

Device name
Trilor Disks, Blocks and Arches
Applicant
Bioloren S.R.L.
Saronno, IT
Received
November 27, 2017
Decision date
February 24, 2018
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
EBF – Material, Tooth Shade, Resin
Device class
Class II (moderate risk)
Regulation
21 CFR 872.3690
Specialty
Dental

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Questions and answers

When was Trilor Disks, Blocks and Arches cleared by the FDA?

Trilor Disks, Blocks and Arches (K173643) received a 510(k) decision of Substantially Equivalent on February 24, 2018, 89 days after the submission was received.

What is the product code of K173643?

The FDA product code is EBF – Material, Tooth Shade, Resin, a Class II (moderate risk) device regulated under 21 CFR 872.3690.