510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K771889Substantially Equivalent

Uniolite

Espe Dental Products, Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K771889 is the FDA 510(k) clearance record for UNIOLITE, a class II device, cleared for Espe Dental Products on under FDA product code EBZ (Activator, Ultraviolet, For Polymerization). FDA records list 8 510(k) clearances for Espe Dental Products, from to . As of , FDA records show no recalls naming K771889.

Clearance record

Decision date
Received
(14 days to decision)
Product code
EBZ Activator, Ultraviolet, For Polymerization
Regulation
21 CFR 872.6070
Device class
Class II
Review panel
Dental
Applicant
Espe Dental Products 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code EBZ

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