510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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DEN110004Unknown

Cabochon System

Cabochon Aesthetics, Inc., Menlo Park CA / Post-NSE, Unknown
FDA source (opens on fda.gov)

DEN110004 is the FDA 510(k) clearance record for CABOCHON SYSTEM, a class II device, cleared for Cabochon Aesthetics, Inc. on under FDA product code OUP (Powered Surgical Instrument For Improvement In The Appearance Of Cellulite). FDA's definition for product code OUP reads: "Used for controlled release of subcutaneous tissue for improvement in the appearance of cellulite". FDA records list 2 510(k) clearances for Cabochon Aesthetics, Inc., from to . As of , FDA records show no recalls naming DEN110004.

Clearance record

Decision date
Received
(620 days to decision)
Product code
OUP Powered Surgical Instrument For Improvement In The Appearance Of Cellulite
Regulation
21 CFR 878.4790
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Cabochon Aesthetics, Inc. 127 Independence Dr., Menlo Park CA
Third party review
No

Clearances, product code OUP

Trailing 12 months

FDA records hold no clearances under product code OUP in the trailing twelve months.

FDA records show no clearances under product code OUP in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code OUP, 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