510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K180581Substantially Equivalent

UV Lamps for Sunlamp Products

Feilo Sylvania Germany GmbH, Erlangen, DE / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K180581 is the FDA 510(k) clearance record for UV Lamps for Sunlamp Products, a class II device, cleared for Feilo Sylvania Germany GmbH on under FDA product code LEJ (Booth, Sun Tan). FDA records list one 510(k) clearance for Feilo Sylvania Germany GmbH. As of , FDA records show no recalls naming K180581.

Clearance record

Decision date
Received
(113 days to decision)
Product code
LEJ Booth, Sun Tan
Regulation
21 CFR 878.4635
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Feilo Sylvania Germany GmbH Graf-Zepplin-Str.9, Erlangen, DE
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