510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K111049Substantially Equivalent

Mobile Versa Light

Medtek Lighting, Knoxville TN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K111049 is the FDA 510(k) clearance record for MOBILE VERSA LIGHT, a class II device, cleared for Medtek Lighting Corp on under FDA product code FTC (Light, Ultraviolet, Dermatological). FDA records list 3 510(k) clearances for Medtek Lighting Corp, from to . As of , FDA records show no recalls naming K111049.

Clearance record

Decision date
Received
(406 days to decision)
Product code
FTC Light, Ultraviolet, Dermatological
Regulation
21 CFR 878.4630
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Medtek Lighting Corp 1131 Anthem View Ln., Knoxville TN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code FTC

Trailing 12 months
2 clearances under product code FTC 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 FTC, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20261
April 20260
May 20261
June 20260
July 20260
August 20260
September 20260
October 20260