# K102076: Liquiband Dual, Model LBD 001

- Pathway: 510(k) (Traditional)
- Applicant: Medlogic Global Limited
- Decided: Feb 18, 2011 after 207 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: 3 generations back to P010002 (2002). 3 ancestors in all.
No later device cites it as a predicate yet.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K100284: Liquiband Ultima, Lut 003, Medlogic Global Limited (2010) Summary page 1.

## Indications for use
LiquiBand Dual 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 Dual topical skin adhesive may be used in conjunction with, but not in place of, deep dermal stitches.

Source page: https://510kreport.com/device/K102076
Methodology: https://510kreport.com/methodology