Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Triton Technology, Inc. — Predicate Candidate Screening
4 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K932142 | SUCTION GUILLOTINE DEVICE | Triton Technology, Inc. | 1993-09-24 | 144 | 0 |
| K911448 | MULTIPLE BIOPSY DEVICE-MBX | Triton Technology, Inc. | 1991-04-16 | 32 | 0 |
| K902883 | TISSUE/POLYP TRAP SYSTEM | Triton Technology, Inc. | 1990-09-12 | 72 | 0 |
| K881303 | TRITON MODEL 100 PULSED DOPPLER BLOOD FLOWMETER | Triton Technology, Inc. | 1988-11-29 | 246 | 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