Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Geiger Medical Technologies, Inc. · Predicate Candidate Screening
5 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
56 daysmedian FDA review time
90 days90th percentile
5clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K002341 | THERMAL CAUTERY UNIT, MODEL 150 | Geiger Medical Technologies, Inc. | 2000-10-23 | 83 | 0 |
| K001029 | GEIGER NEEDLE ADAPTER, MODEL 406 | Geiger Medical Technologies, Inc. | 2000-05-23 | 54 | 0 |
| K994075 | GEIGER DISPOSABLE ELECTROSURGICAL ELECTRODE, MODEL 435 | Geiger Medical Technologies, Inc. | 1999-12-27 | 25 | 0 |
| K992149 | GEIGER ELECTROSURGICAL HANDPIECE SHEATH, MODEL 405 | Geiger Medical Technologies, Inc. | 1999-08-19 | 56 | 0 |
| K983852 | BLUE VALUE LINE OF ELECTROSURGICAL ELECTRODES, MODEL #'S 421 | Geiger Medical Technologies, Inc. | 1999-01-28 | 90 | 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