FIBER DISK AND BLOCK PERMANENT, TRINIA— 510(k) K121735

Name: FDA 510(k) clearance K121735
Creator: U.S. Food and Drug Administration
Published: 2013-02-21

Substantially Equivalent

Bioloren S.R.L.

FDA 510(k) clearance K121735 for FIBER DISK AND BLOCK PERMANENT, TRINIA, Substantially Equivalent on 2013-02-21. Applicant: Bioloren S.R.L.. Device class: 2.

Clearance details

Applicant: Bioloren S.R.L.
Product code: Code EBF
Device class: Class 2
Regulation: 21 CFR 872.3690
Advisory panel: Dental
Date received: 2012-06-13
Decision date: 2013-02-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Saronno, Va, IT

Download summary PDF View on FDA.gov ↗

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