510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K943363Substantially Equivalent

Cutiplast Steril

Beiersdorf, Inc., Norwalk CT / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K943363 is the FDA 510(k) clearance record for CUTIPLAST STERIL, cleared for Beiersdorf, Inc. on under FDA product code MGP (Dressing, Wound And Burn, Occlusive). FDA records list 48 510(k) clearances for Beiersdorf, Inc., from to . As of , FDA records show no recalls naming K943363.

Clearance record

Decision date
Received
(245 days to decision)
Product code
MGP Dressing, Wound And Burn, Occlusive
Device class
Unclassified
Review panel
Unknown
Applicant
Beiersdorf, Inc. 360 Dr. Martin Luther King Dr., Norwalk CT
510(k) summary
Summary
Third party review
No

Clearances, product code MGP

Trailing 12 months

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

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