Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Medlogic Global Limited — Predicate Candidate Screening
5 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
207 daysmedian FDA review time
329 days90th percentile
5clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K110184 | LIQUIBAND FLOW CONTROL | Medlogic Global Limited | 2011-12-16 | 329 | 0 |
| K102076 | LIQUIBAND DUAL, MODEL LBD 001 | Medlogic Global Limited | 2011-02-18 | 207 | 0 |
| K100284 | LIQUIBAND ULTIMA, LUT 003 | Medlogic Global Limited | 2010-04-09 | 67 | 0 |
| K031321 | LIQUISHIELD LIQUID BANDAGE, MODEL LSB 0001 | Medlogic Global Limited | 2004-01-21 | 271 | 0 |
| K023163 | LIQUISHIELD-S (0.7G), MODEL LS 0010, LIQUISHIELD-S (2.0G), M | Medlogic Global Limited | 2003-01-13 | 112 | 0 |
Methodology
Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.
Prepared with Atlas
Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda