Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
John F. Greer Co., Inc. — Predicate Candidate Screening
5 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
63 daysmedian FDA review time
79 days90th percentile
5clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K870577 | E-Z LOOP | John F. Greer Co., Inc. | 1987-04-17 | 66 | 0 |
| K870531 | EZ TAC FILTER | John F. Greer Co., Inc. | 1987-04-10 | 63 | 0 |
| K864190 | E-Z HOLD - #4060 | John F. Greer Co., Inc. | 1987-01-14 | 79 | 0 |
| K864188 | E-Z HOLD WITH ADHESIVE BASE.-#4065 | John F. Greer Co., Inc. | 1986-12-04 | 38 | 0 |
| K864189 | ULTRA-GEL - #4083 | John F. Greer Co., Inc. | 1986-12-04 | 38 | 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