Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Sorenson Laboratories, 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) |
|---|---|---|---|---|---|
| K930434 | PLUMEMASTER SMOKE EVACUATION SYSTEM | Sorenson Laboratories, Inc. | 1993-11-16 | 294 | 0 |
| K931356 | SAFE AIR VARI-SPOT HANDPIECE TELESCOPE AND ADAPTOR | Sorenson Laboratories, Inc. | 1993-09-07 | 174 | 0 |
| K920597 | HANDI-LASE CO2 SURGICAL LASER INSTRUMENT | Sorenson Laboratories, Inc. | 1992-06-04 | 114 | 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