Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Lccs Products Limited · Predicate Candidate Screening
5 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
239 daysmedian FDA review time
346 days90th percentile
5clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K191293 | LCCS VC-S RF Cannula | Lccs Products Limited | 2020-01-24 | 255 | 0 |
| K152642 | LCCS Disposable RF Electrode, LCCS Reusable RF Electrode | Lccs Products Limited | 2016-08-26 | 346 | 0 |
| K131006 | ANESTHESIA CONDUCTION NEEDLES | Lccs Products Limited | 2013-12-06 | 239 | 0 |
| K132136 | SINGLE USE GROUNDING PAD | Lccs Products Limited | 2013-09-06 | 57 | 0 |
| K112231 | LCCS INSULATED SPINAL NEEDLE (RF CANNULA) | Lccs Products Limited | 2011-08-19 | 15 | 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