Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Vapocoolshot, Inc. — Predicate Candidate Screening
3 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K243654 | DentalJect | Vapocoolshot, Inc. | 2025-05-30 | 185 | 0 |
| K201248 | Syringe Holder accessory | Vapocoolshot, Inc. | 2020-08-12 | 93 | 0 |
| K193349 | Vapocoolshot Mist | Vapocoolshot, Inc. | 2020-04-14 | 133 | 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