510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K101366Substantially Equivalent

I-Lipo, Models A00-1238 (230V), A00-1239 (120V)

Chromogenex Technologies Limited, Llanelli, Carmarthenshire, GB / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K101366 is the FDA 510(k) clearance record for I-LIPO, MODELS A00-1238 (230V), A00-1239 (120V), a class II device, cleared for Chromogenex Technologies, Ltd. on under FDA product code NUV (Massager, Vacuum, Light Induced Heating). FDA's definition for product code NUV reads: "The device is intended to temporarily alter the appearance of cellulite". FDA records list 3 510(k) clearances for Chromogenex Technologies, Ltd., from to . As of , FDA records show no recalls naming K101366.

Clearance record

Decision date
Received
(123 days to decision)
Product code
NUV Massager, Vacuum, Light Induced Heating
Regulation
21 CFR 878.4810
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Chromogenex Technologies, Ltd. Units 1& 2 Heol Rhosyn, Llanelli, Carmarthenshire, GB
510(k) summary
Summary PDF
Third party review
No

Clearances, product code NUV

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