PMA
P220024: LIQUIFIX FIX8 Hernia Mesh Fixation (HMF) Device, LIQUIFIX Precision Open Hernia Mesh Fixation Device
FDA PMA · Tissue adhesive internal use · Advanced Medical Solutions Limited
Key facts
| PMA number | P220024 |
|---|---|
| Trade name | LIQUIFIX FIX8 Hernia Mesh Fixation (HMF) Device, LIQUIFIX Precision Open Hernia Mesh Fixation Device |
| Generic name | Tissue adhesive internal use |
| Applicant | Advanced Medical Solutions Limited |
| Owner/operator | ADVANCED MEDICAL SOLUTIONS GROUP PLC |
| Product code | PLJ |
| Approval date | Jun 2, 2023 |
| Docket number | 23M-2807 |
| Notice date | Jul 28, 2023 |
| Establishment registration | 9617175 |
| FEI number | 3010571423 |
At a glance
- 1–9 Supplements
- Jan 14, 2026 Latest supplement decision
- No Withdrawn
- Yes Summary of safety and effectiveness on file
- 1–9 UDI device identifiers (GUDID)
- None MAUDE adverse event reports
- None Recall events
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About PMA approvals
Premarket approval (PMA) is the FDA's most stringent review pathway, required for most Class III devices that support or sustain life or present a potentially unreasonable risk.
Source: U.S. Food and Drug Administration (FDA), Premarket Approval (PMA) database · Source date: