# K100284: Liquiband Ultima, Lut 003

- Pathway: 510(k) (Traditional)
- Applicant: Medlogic Global Limited
- Decided: Apr 9, 2010 after 67 days
- Product code: MPN (Tissue Adhesive For The Topical Approximation Of Skin)
- Device class: 2
- Regulation: 21 CFR 878.4010
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to P010002 (2002). 2 ancestors in all.
9 later devices descend from it; 3 cite it directly.
0 of 12 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K083531: Liquiband Ultima, Model LB0004, Medlogic Global, Ltd. (2009) Summary page 1.

## Most influential descendants
- K110184: Liquiband Flow Control (2011), 6 descendants of its own
- K122446: Liquidband Flow Control (2012), 5 descendants of its own
- K123133: Barle Tissue Adhesive (2013), 3 descendants of its own
- K132243: Barle Tissue Adhesive 2 (2013), 2 descendants of its own
- K151182: LiquiBand Exceed (2015), 1 descendant of its own

## Indications for use
LiquiBand Ultima topical skin adhesive is intended for topical applications only, to hold closed easily approximated skin edges of wounds from surgical incisions, including punctures from minimally invasive surgery and simple, thoroughly cleansed, trauma induced lacerations. LiquiBand Ultima topical skin adhesive may be used in conjunction with, but not in place of, deep dermal stitches.

Source page: https://510kreport.com/device/K100284
Methodology: https://510kreport.com/methodology