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
K152412Substantially Equivalent

T-32;T-40;T-44;T-52;T-72;Tt-50

Tanses Technologies, Inc., Laval Quebec, CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K152412 is the FDA 510(k) clearance record for T-32;T-40;T-44;T-52;T-72;TT-50, a class II device, cleared for Tanses Technologies, Inc. on under FDA product code LEJ (Booth, Sun Tan). FDA records list 3 510(k) clearances for Tanses Technologies, Inc., from to . As of , FDA records show no recalls naming K152412.

Clearance record

Decision date
Received
(247 days to decision)
Product code
LEJ Booth, Sun Tan
Regulation
21 CFR 878.4635
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Tanses Technologies, Inc. 4450 Hwy. 13, Laval Quebec, CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code LEJ

Trailing 12 months

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

FDA records show no clearances under product code LEJ in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code LEJ, 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