510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
Medical Device
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K072035Substantially Equivalent

Resolve Uvb Phototherapy System

Allux Medical, Menlo Park CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K072035 is the FDA 510(k) clearance record for RESOLVE UVB PHOTOTHERAPY SYSTEM, a class II device, cleared for Allux Medical on under FDA product code FTC (Light, Ultraviolet, Dermatological). FDA records list one 510(k) clearance for Allux Medical. As of , FDA records show no recalls naming K072035.

Clearance record

Decision date
Received
(83 days to decision)
Product code
FTC Light, Ultraviolet, Dermatological
Regulation
21 CFR 878.4630
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Allux Medical 1430 O'Brien Dr., Menlo Park CA
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