Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
Tillotson 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) |
|---|---|---|---|---|---|
| K891939 | NON STERILE EXAM GLOVES ( TILLOTSON RUBBER CO.) | Tillotson Corp. | 1989-07-14 | 108 | 0 |
| K891940 | PATIENT EXAM GLOVES (MFG. MOSS POINT GLOVE CO.) | Tillotson Corp. | 1989-07-14 | 108 | 0 |
| K893901 | LATEX EXAMINATION GLOVES | Tillotson Corp. | 1989-07-14 | 45 | 0 |
| K893018 | HPI NON STERILE EXAM GLOVES | Tillotson Corp. | 1989-06-22 | 71 | 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