510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K021083Substantially Equivalent

Veracam

Lumalite, Inc., Los Angeles CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K021083 is the FDA 510(k) clearance record for VERACAM, a class I device, cleared for Lumalite, Inc. on under FDA product code EIA (Unit, Operative Dental). FDA records list 3 510(k) clearances for Lumalite, Inc., from to . As of , FDA records show no recalls naming K021083.

Clearance record

Decision date
Received
(149 days to decision)
Product code
EIA Unit, Operative Dental
Regulation
21 CFR 872.6640
Device class
Class I
Review panel
Dental
Applicant
Lumalite, Inc. 11661 San Vicente Blvd., Los Angeles CA
510(k) summary
Statement
Third party review
No

Clearances, product code EIA

Trailing 12 months
2 clearances under product code EIA in the twelve months to October 2026, November 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code EIA, trailing twelve months
MonthClearances
November 20251
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20261
September 20260
October 20260