510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K241151Substantially Equivalent

Luxen 5G

Dentalmax Co., Ltd, Cheonan-Si, KR / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K241151 is the FDA 510(k) clearance record for LUXEN 5G, a class II device, cleared for Dentalmax Co., Ltd. on under FDA product code EIH (Powder, Porcelain). FDA records list 3 510(k) clearances for Dentalmax Co., Ltd., from to . As of , FDA records show no recalls naming K241151.

Clearance record

Decision date
Received
(158 days to decision)
Product code
EIH Powder, Porcelain
Regulation
21 CFR 872.6660
Device class
Class II
Review panel
Dental
Applicant
Dentalmax Co., Ltd. 50-7, Pungsesandan 2-Ro, Cheonan-Si, KR
510(k) summary
Summary PDF
Third party review
No

Clearances, product code EIH

Trailing 12 months
13 clearances under product code EIH in the twelve months to October 2026, June 2026 the highest month at 3.
Show the numbers
Monthly 510(k) clearances under FDA product code EIH, trailing twelve months
MonthClearances
November 20250
December 20251
January 20262
February 20260
March 20262
April 20261
May 20261
June 20263
July 20262
August 20261
September 20260
October 20260