Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Stierlen-Maquet AG — Predicate Candidate Screening
10 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
31 daysmedian FDA review time
286 days90th percentile
10clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K970807 | MOBILE OPERATING TABLE 1132.01 | Stierlen-Maquet AG | 1997-03-14 | 9 | 0 |
| K926525 | BETASTAR 1131.02 MOBILE OPERATING TABLE | Stierlen-Maquet AG | 1993-10-12 | 286 | 0 |
| K920890 | OPERATING TABLE SYSTEM-BETAMAQUET 1140 | Stierlen-Maquet AG | 1992-07-02 | 141 | 0 |
| K883613 | OPER. TABLE FOR PERCUTAN. TRANS. CORONARY ANGIO. | Stierlen-Maquet AG | 1988-09-15 | 24 | 0 |
| K873274 | PLASTER TABLE 1418 | Stierlen-Maquet AG | 1987-09-17 | 31 | 0 |
| K873276 | EXTENSION DEVICE 1416 | Stierlen-Maquet AG | 1987-09-17 | 31 | 0 |
| K873275 | EXTENSION TABLE 1417 | Stierlen-Maquet AG | 1987-09-17 | 31 | 0 |
| K873273 | ORTHOPAEDIC TABLE 1420 | Stierlen-Maquet AG | 1987-09-17 | 31 | 0 |
| K873272 | ENDOSCOPY TABLE 1532 ENDOSTAR | Stierlen-Maquet AG | 1987-09-08 | 22 | 0 |
| K843134 | MOBILE OPERATING TABLE HEIDELBERGS 1130 | Stierlen-Maquet AG | 1984-09-07 | 29 | 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