Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
Stuckenbrock Medizintechnik GmbH · 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) |
|---|---|---|---|---|---|
| K171624 | IXOS Radius Plate System | Stuckenbrock Medizintechnik GmbH | 2018-03-29 | 300 | 0 |
| K171628 | HBS2 Headless Bone Screw | Stuckenbrock Medizintechnik GmbH | 2018-01-12 | 224 | 0 |
| K042902 | HERBERT ULNAR HEAD PROSTHESIS SYSTEM | Stuckenbrock Medizintechnik GmbH | 2004-12-27 | 68 | 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