510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K933265Substantially Equivalent

Acu-Dispo-Ce(tm)

Acuderm, Inc., Ft. Lauderdale FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K933265 is the FDA 510(k) clearance record for ACU-DISPO-CE(TM), a class I device, cleared for Acuderm, Inc. on under FDA product code MDM (Instrument, Manual, Surgical, General Use). FDA records list 13 510(k) clearances for Acuderm, Inc., from to . As of , FDA records show no recalls naming K933265.

Clearance record

Decision date
Received
(244 days to decision)
Product code
MDM Instrument, Manual, Surgical, General Use
Regulation
21 CFR 878.4800
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Acuderm, Inc. 5370 NW 35th Ter., Ft. Lauderdale FL
510(k) summary
Statement
Third party review
No

Clearances, product code MDM

Trailing 12 months

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

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