Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Closure Medical Corp. · Predicate Candidate Screening
4 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| DEN090005 | PRINEO SKIN CLOSURE SYSTEM | Closure Medical Corp. | 2010-04-30 | 402 | 0 |
| K002338 | LIQUIDERM LIQUID ADHESIVE BANDAGE | Closure Medical Corp. | 2001-01-29 | 181 | 0 |
| K991923 | SOOTHE-N-SEAL CANKER SORE RELIEF | Closure Medical Corp. | 1999-09-02 | 87 | 0 |
| K980159 | OCTYLDENT (2-OCTYL CYANOACRYLATE), 02A01 | Closure Medical Corp. | 1998-04-09 | 83 | 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