510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K233307Substantially Equivalent

Intensity Pulsed Light Therapy System

Beijing Adss Development Co., Ltd., Beijing, CN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K233307 is the FDA 510(k) clearance record for Intensity Pulsed Light Therapy System, a class II device, cleared for Beijing Adss Development Co., Ltd. on under FDA product code ONF (Powered Light Based Non-Laser Surgical Instrument With Thermal Effect). FDA's definition for product code ONF reads: "A light based non-laser device that provides thermal effect including broad spectrum source devices such as intense pulse light (ipl). Typically, indicated to be used in medical specialties of general and plastic surgery and of...". FDA records list 10 510(k) clearances for Beijing Adss Development Co., Ltd., from to . As of , FDA records show no recalls naming K233307.

Clearance record

Decision date
Received
(168 days to decision)
Product code
ONF Powered Light Based Non-Laser Surgical Instrument With Thermal Effect
Regulation
21 CFR 878.4810
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Beijing Adss Development Co., Ltd. Rm. 609, F6, Bldg. 13, Yard 5 Tianhua St.,, Beijing, CN
510(k) summary
Statement
Third party review
No

Clearances, product code ONF

Trailing 12 months
1 clearance under product code ONF in the twelve months to October 2026, June 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code ONF, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20261
July 20260
August 20260
September 20260
October 20260