Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Teledyne Getz — Predicate Candidate Screening
5 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
78 daysmedian FDA review time
106 days90th percentile
5clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K923675 | DENSPRO MEDIUM MINT PROPHY PASTE | Teledyne Getz | 1992-11-05 | 106 | 0 |
| K923674 | DENSPRO COARSE MINT PROPHY PASTE | Teledyne Getz | 1992-11-05 | 106 | 0 |
| K903568 | SUPER STRENGTH DENTURE ADHESIVE CREAM | Teledyne Getz | 1990-10-24 | 78 | 0 |
| K901938 | SUPER STRENGTH DENTURE ADHESIVE CREAM | Teledyne Getz | 1990-06-06 | 37 | 0 |
| K901239 | TELEDYNE GETZ'S DISPOSABLE PROPHY ANGLE | Teledyne Getz | 1990-05-15 | 61 | 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