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
K001179Substantially Equivalent

Super Nova, Acubeam

Light Force Therapy, Inc., Payton CO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K001179 is the FDA 510(k) clearance record for SUPER NOVA, ACUBEAM, a class II device, cleared for Light Force Therapy, Inc. on under FDA product code ILY (Lamp, Infrared, Therapeutic Heating). FDA records list 2 510(k) clearances for Light Force Therapy, Inc., from to . As of , FDA records show no recalls naming K001179.

Clearance record

Decision date
Received
(199 days to decision)
Product code
ILY Lamp, Infrared, Therapeutic Heating
Regulation
21 CFR 890.5500
Device class
Class II
Review panel
Physical Medicine
Applicant
Light Force Therapy, Inc. 17725 Cleese Ct., Payton CO
510(k) summary
Statement
Third party review
No

Clearances, product code ILY

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