LiquiBand XL— 510(k) K211878

Clearance details

Applicant

Advanced Medical Solutions Limited

Product code

Code OMD

Device class

Class 2

Regulation

21 CFR 878.4011

Advisory panel

General, Plastic Surgery

Date received

2021-06-21

Decision date

2022-05-23

Decision

Substantially Equivalent

Clearance type

Traditional

Location

Plymouth, GB

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• K223310 — Antimicrobial Silicone PHMB Foam Wound Dressing2023-04-05
• K183570 — LiquiBand Plus2020-03-09
• K110458 — SILVER ANTIMICROBIAL WOUND GEL2011-03-14
• K091013 — SILVER PU ANTIBACTERIAL FOAM DRESSING - NON ADHERENT AND ISLAND2009-07-30
• K090453 — SILVER ALGINATE 11 WOUND DRESSING2009-02-26

Injury

1,134

Total

1,134

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →