Stierlen-Maquet AG: FDA filings under this applicant name
FDA lists 10 510(k) clearances under the applicant name “Stierlen-Maquet AG” (first 1984, latest 1997), across 4 product codes in 1 review panel. Median 510(k) review time under this name: 31 days. Related companies, subsidiaries and acquired businesses that file under other applicant names are counted on their own pages, not here.
510(k) clearances per year
| Year | Clearances | Median review days |
|---|---|---|
| 2012 | 0 | — |
| 2013 | 0 | — |
| 2014 | 0 | — |
| 2015 | 0 | — |
| 2016 | 0 | — |
| 2017 | 0 | — |
| 2018 | 0 | — |
| 2019 | 0 | — |
| 2020 | 0 | — |
| 2021 | 0 | — |
| 2022 | 0 | — |
| 2023 | 0 | — |
| 2024 | 0 | — |
| 2025 | 0 | — |
| 2026 | 0 | — |
Top product codes
| Product code | Device | Submissions | 510(k) clearances |
|---|---|---|---|
| JEB | Table, Surgical With Orthopedic Accessories, Manual | 4 | 4 |
| GDC | Table, Operating-Room, Electrical | 3 | 3 |
| FQO | Table, Operating-Room, Ac-Powered | 2 | 2 |
| BWN | Table And Attachments, Operating-Room | 1 | 1 |
Review panels
Most recent Stierlen-Maquet AG 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K970807 | MOBILE OPERATING TABLE 1132.01 | GDC | 1997-03-14 | 9 |
| K926525 | BETASTAR 1131.02 MOBILE OPERATING TABLE | FQO | 1993-10-12 | 286 |
| K920890 | OPERATING TABLE SYSTEM-BETAMAQUET 1140 | FQO | 1992-07-02 | 141 |
| K883613 | OPER. TABLE FOR PERCUTAN. TRANS. CORONARY ANGIO. | GDC | 1988-09-15 | 24 |
| K873276 | EXTENSION DEVICE 1416 | JEB | 1987-09-17 | 31 |
| K873275 | EXTENSION TABLE 1417 | JEB | 1987-09-17 | 31 |
| K873274 | PLASTER TABLE 1418 | JEB | 1987-09-17 | 31 |
| K873273 | ORTHOPAEDIC TABLE 1420 | JEB | 1987-09-17 | 31 |
| K873272 | ENDOSCOPY TABLE 1532 ENDOSTAR | BWN | 1987-09-08 | 22 |
| K843134 | MOBILE OPERATING TABLE HEIDELBERGS 1130 | GDC | 1984-09-07 | 29 |
Recalls
openFDA lists no recalls under a recalling firm named Stierlen-Maquet AG.
Recalling firms are matched to this applicant name by name only (same normalization), so related entities that recall under another name are not counted. A recall count says nothing about how safe one company's devices are compared with another's.
Frequently asked questions
How many FDA 510(k) clearances are listed under Stierlen-Maquet AG?
FDA lists 10 510(k) clearances under the applicant name “Stierlen-Maquet AG” (first 1984, latest 1997), across 4 product codes in 1 review panel. Filings under other applicant names, such as subsidiaries, are not included.
How long has FDA taken to clear 510(k)s filed by Stierlen-Maquet AG?
The median time from FDA receipt to decision across 510(k)s cleared under the name Stierlen-Maquet AG is 31 days.
Which FDA product codes appear under Stierlen-Maquet AG?
The most frequent FDA product codes under this applicant name are JEB (Table, Surgical With Orthopedic Accessories, Manual, 4); GDC (Table, Operating-Room, Electrical, 3); FQO (Table, Operating-Room, Ac-Powered, 2).
Next steps
- See all 10 Stierlen-Maquet AG clearances with predicates and recalls
- Run predicate analysis for product code JEB, Stierlen-Maquet AG's most frequent
Data from openFDA (510(k), PMA, De Novo, device recalls), ClinicalTrials.gov and SEC company tickers. Each page covers one FDA applicant name, with punctuation and legal suffixes removed; filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.