Medlogic Global Limited: FDA filings under this applicant name
FDA lists 5 510(k) clearances under the applicant name “Medlogic Global Limited” (first 2003, latest 2011), across 2 product codes in 1 review panel. Median 510(k) review time under this name: 207 days. Related companies, subsidiaries and acquired businesses that file under other applicant names are counted on their own pages, not here.
510(k) clearances per year
| Year | Clearances | Median review days |
|---|---|---|
| 2012 | 0 | — |
| 2013 | 0 | — |
| 2014 | 0 | — |
| 2015 | 0 | — |
| 2016 | 0 | — |
| 2017 | 0 | — |
| 2018 | 0 | — |
| 2019 | 0 | — |
| 2020 | 0 | — |
| 2021 | 0 | — |
| 2022 | 0 | — |
| 2023 | 0 | — |
| 2024 | 0 | — |
| 2025 | 0 | — |
| 2026 | 0 | — |
Top product codes
| Product code | Device | Submissions | 510(k) clearances |
|---|---|---|---|
| MPN | Tissue Adhesive For The Topical Approximation Of Skin | 3 | 3 |
| KMF | Bandage, Liquid | 2 | 2 |
Review panels
Most recent Medlogic Global Limited 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K110184 | LIQUIBAND FLOW CONTROL | MPN | 2011-12-16 | 329 |
| K102076 | LIQUIBAND DUAL, MODEL LBD 001 | MPN | 2011-02-18 | 207 |
| K100284 | LIQUIBAND ULTIMA, LUT 003 | MPN | 2010-04-09 | 67 |
| K031321 | LIQUISHIELD LIQUID BANDAGE, MODEL LSB 0001 | KMF | 2004-01-21 | 271 |
| K023163 | LIQUISHIELD-S (0.7G), MODEL LS 0010, LIQUISHIELD-S (2.0G), MODEL LS 0020 | KMF | 2003-01-13 | 112 |
Recalls
openFDA lists no recalls under a recalling firm named Medlogic Global Limited.
Recalling firms are matched to this applicant name by name only (same normalization), so related entities that recall under another name are not counted. A recall count says nothing about how safe one company's devices are compared with another's.
Device clinical trials
An industry sponsor named Medlogic Global Limited is the lead sponsor of 1 device studies on ClinicalTrials.gov (0 active or recruiting). Most recent:
- NCT00762905: Clinical Trial of MedLogic LiquiBand Laparoscopic Versus Dermabond in the Closure of Surgical Incisions (Completed, started 2006-04)
Other FDA applicant names starting with the same word
FDA records these as separate applicants. Some may belong to the same corporate group and some may not; their filings are not included in the counts above.
- Medlogic Global Corp. (3 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Medlogic Global Limited?
FDA lists 5 510(k) clearances under the applicant name “Medlogic Global Limited” (first 2003, latest 2011), across 2 product codes in 1 review panel. Filings under other applicant names, such as subsidiaries, are not included.
How long has FDA taken to clear 510(k)s filed by Medlogic Global Limited?
The median time from FDA receipt to decision across 510(k)s cleared under the name Medlogic Global Limited is 207 days.
Which FDA product codes appear under Medlogic Global Limited?
The most frequent FDA product codes under this applicant name are MPN (Tissue Adhesive For The Topical Approximation Of Skin, 3); KMF (Bandage, Liquid, 2).
Next steps
- See all 5 Medlogic Global Limited clearances with predicates and recalls
- Run predicate analysis for product code MPN, Medlogic Global Limited's most frequent
Data from openFDA (510(k), PMA, De Novo, device recalls), ClinicalTrials.gov and SEC company tickers. Each page covers one FDA applicant name, with punctuation and legal suffixes removed; filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.