510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K162721Substantially Equivalent

Stimucel System, Stimucel Generator, Stimucel Treatment Wand, Stimucel Applicator

Alliqua Biomedical, Inc., Eden Prairie MN / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K162721 is the FDA 510(k) clearance record for Stimucel System, Stimucel Generator, Stimucel Treatment Wand, Stimucel Applicator, a class II device, cleared for Alliqua Biomedical, Inc. on under FDA product code NRB (Wound Cleaner, Ultrasound). FDA's definition for product code NRB reads: "The ultrasound wound cleaner/mild debridement system is a device that delivers a cleaning fluid to the wound that is pulsed using low power ultrasound radiation. The device is intended to clean and mildly debride wounds. The ultrasound...". FDA records list 2 510(k) clearances for Alliqua Biomedical, Inc., from to . As of , FDA records show no recalls naming K162721.

Clearance record

Decision date
Received
(84 days to decision)
Product code
NRB Wound Cleaner, Ultrasound
Regulation
21 CFR 878.4410
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Alliqua Biomedical, Inc. 11495 Valley View Rd., Eden Prairie MN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code NRB

Trailing 12 months

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

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