510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K131623Substantially Equivalent

Smartdop Xt

Koven Technology, Inc., Houston TX / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K131623 is the FDA 510(k) clearance record for SMARTDOP XT, a class II device, cleared for Koven Technology, Inc. on under FDA product code JOP (Transducer, Ultrasonic). FDA records list 18 510(k) clearances for Koven Technology, Inc., from to . As of , FDA records show no recalls naming K131623.

Clearance record

Decision date
Received
(227 days to decision)
Product code
JOP Transducer, Ultrasonic
Regulation
21 CFR 870.2880
Device class
Class II
Review panel
Cardiovascular
Applicant
Koven Technology, Inc. 11874 S. Evelyn Cir., Houston TX
510(k) summary
Summary PDF
Third party review
No

Clearances, product code JOP

Trailing 12 months

FDA records hold no clearances under product code JOP in the trailing twelve months.

FDA records show no clearances under product code JOP in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code JOP, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260