510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K211854Substantially Equivalent

VITA Akzent LC

Vita Zahnfabrik GmbH H Rauter & Co, Bad Sackingen, DE / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K211854 is the FDA 510(k) clearance record for VITA Akzent LC, a class II device, cleared for Vita Zahnfabrik GmbH H Rauter & CO on under FDA product code EBD (Coating, Filling Material, Resin). FDA records list 3 510(k) clearances for Vita Zahnfabrik GmbH H Rauter & CO, from to . As of , FDA records show no recalls naming K211854.

Clearance record

Decision date
Received
(159 days to decision)
Product code
EBD Coating, Filling Material, Resin
Regulation
21 CFR 872.3310
Device class
Class II
Review panel
Dental
Applicant
Vita Zahnfabrik GmbH H Rauter & CO Spitelgasse 3, Bad Sackingen, DE
510(k) summary
Summary PDF
Third party review
No

Clearances, product code EBD

Trailing 12 months
1 clearance under product code EBD in the twelve months to October 2026, April 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code EBD, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20261
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260