Trilor Disks, Blocks and Arches
K-Number: K173643 · 2018-02-24
Device Summary
Frequently Asked Questions
What is the Trilor Disks, Blocks and Arches?
Trilor Disks, Blocks and Arches is a medical device that received FDA 510(k) clearance on 2018-02-24. The listed applicant is Bioloren S.R.L.. The 510(k) number is K173643.
When did Trilor Disks, Blocks and Arches receive FDA 510(k) clearance?
Trilor Disks, Blocks and Arches received FDA 510(k) clearance on 2018-02-24, under 510(k) number K173643.
Who is the listed applicant for Trilor Disks, Blocks and Arches?
The FDA 510(k) record lists Bioloren S.R.L. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Trilor Disks, Blocks and Arches?
The FDA product code for Trilor Disks, Blocks and Arches is EBF.
Related Devices (Code: EBF)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.