Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Feel Tech — 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) |
|---|---|---|---|---|---|
| K092831 | DISPOSABLE HYPODERMIC NEEDLE | Feel Tech | 2010-01-14 | 121 | 0 |
| K080904 | FEEL-FINE INSULIN PEN NEEDLE | Feel Tech | 2008-06-04 | 64 | 7 |
| K070917 | FEEL-JECT INSULIN SYRINGE | Feel Tech | 2007-06-20 | 79 | 1 |
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