Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Tillotson Rubber Co., Inc. · Predicate Candidate Screening
6 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
60 daysmedian FDA review time
280 days90th percentile
6clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K905765 | PILGRIM NITRILE LATEX GLOVES (VARIOUS TYPES) | Tillotson Rubber Co., Inc. | 1991-02-25 | 60 | 0 |
| K903756 | STERILE PATIENT EXAMINATION GLOVES | Tillotson Rubber Co., Inc. | 1990-09-05 | 23 | 0 |
| K903607 | POWDER FREE, NON-STERILE EXAMINATION GLOVES | Tillotson Rubber Co., Inc. | 1990-08-17 | 10 | 0 |
| K894828 | HPI ORTHO SURGEONS' GLOVE | Tillotson Rubber Co., Inc. | 1990-05-07 | 280 | 0 |
| K780181 | GLOVES, FLOOR | Tillotson Rubber Co., Inc. | 1978-02-21 | 18 | 0 |
| K770704 | GLOVES, SURGEONS, LATEX | Tillotson Rubber Co., Inc. | 1977-06-24 | 67 | 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