510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K052660Substantially Equivalent

Model 672-Bd, Home Uvb Light Source (Jordan Light); Model 2400, 4 (6 Foot) Ho UV Light Source; Model 2600, 6 (6 Foot) Ho

The Richmond Light Co., Richmond VA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K052660 is the FDA 510(k) clearance record for MODEL 672-BD, HOME UVB LIGHT SOURCE (JORDAN LIGHT); MODEL 2400, 4 (6 FOOT) HO UV LIGHT SOURCE; MODEL 2600, 6 (6 FOOT) HO, a class II device, cleared for The Richmond Light Co. on under FDA product code FTC (Light, Ultraviolet, Dermatological). FDA records list 2 510(k) clearances for The Richmond Light Co., from to . As of , FDA records show no recalls naming K052660.

Clearance record

Decision date
Received
(20 days to decision)
Product code
FTC Light, Ultraviolet, Dermatological
Regulation
21 CFR 878.4630
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
The Richmond Light Co. 2301 Falkirk Dr., Richmond VA
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