Liquiband Flow Control

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K110184 ↗

FDA Product Code

MPN

Device Class

Class II

Regulation

21 CFR Part 878.4010

Advisory Committee

General, Plastic Surgery

FDA Decision

SESE Substantially Equivalent

• LiquiBand Dental

  Class II

  FDA 510(k) K993556 Active Cleared 3 Jan 2000

• Liquishield Liquid Bandage, Model Lsb 0001

  Class I

  FDA 510(k) K031321 Active Cleared 21 Jan 2004

• Liquiband Ultima Lut 003

  Class II

  FDA 510(k) K100284 Active Cleared 9 Apr 2010

• Liquiband Ultima, Model LB0004

  Class II

  FDA 510(k) K083531 Active Cleared 12 Feb 2009

• Liquishield-S (0.7g), Model Ls 0010, Liquishield-S (2.0g), Model Ls 0020

  Class I

  FDA 510(k) K023163 Active Cleared 13 Jan 2003

• Liquiband Dual, Model Lbd 001

  Class II

  FDA 510(k) K102076 Active Cleared 18 Feb 2011

See all devices from Medlogic Global Corp. →

• What is the Liquiband Flow Control used for?

  The Liquiband Flow Control is a tissue adhesive designed for the topical approximation of skin during surgical procedures, specifically intended for use in general and plastic surgery settings.

• Is the Liquiband Flow Control single-use or reusable?

  The Liquiband Flow Control is supplied in a single-use format and is not MRI safe, meaning it should be discarded after a single application and cannot be used in MRI environments.

• What is the regulatory status of the Liquiband Flow Control?

  The Liquiband Flow Control is authorized under FDA 510K clearance with product code MPN, having been determined to be substantially equivalent to predicate devices for tissue adhesives used in skin approximation.

• How is the Liquiband Flow Control applied during procedures?

  The Liquiband Flow Control is designed to provide controlled application during surgical procedures, allowing precise delivery of the adhesive for effective skin approximation in general and plastic surgery settings.