510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K101710Substantially Equivalent

Luxatemp Ultra /Star

Dmg USA, Inc., Ayer MA / Abbreviated, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K101710 is the FDA 510(k) clearance record for LUXATEMP ULTRA /STAR, a class II device, cleared for Dmg USA, Inc. on under FDA product code EBG (Crown And Bridge, Temporary, Resin). FDA records list 28 510(k) clearances for Dmg USA, Inc., from to . As of , FDA records show no recalls naming K101710.

Clearance record

Decision date
Received
(103 days to decision)
Product code
EBG Crown And Bridge, Temporary, Resin
Regulation
21 CFR 872.3770
Device class
Class II
Review panel
Dental
Applicant
Dmg USA, Inc. 5 Whitcomb Ave., Ayer MA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code EBG

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