Morpheus AG
Spaichingen Baden-Wurttemberg, DE
MORPHEUS AG appears in FDA device records in Spaichingen Baden-Wurttemberg, DE. FDA records list 3 510(k) clearances between and , no PMA records and 2 registered establishments. As of , FDA records show no recalls for this company, and at least one establishment registration is current.
FDA records held for this company
510(k) clearance history
FDA records hold 3 510(k) clearances for Morpheus AG between 2021 and 2023. The busiest year on record is 2021, with 1. The most recent is 2023, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2021 | 1 |
| 2022 | 1 |
| 2023 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K230256 | Rebellion, Phantom Multi-Bite Kerrison Rongeur | HAE | Substantially Equivalent | |
| K221818 | Rebellion; Phantom Multi-Bite Kerrison Rongeur | HAE | Substantially Equivalent | |
| K200768 | Rebellion, Phantom Multi-Bite Kerrison Rongeur | HAE | Substantially Equivalent |
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 3016450051 | 3016450051 | MORPHEUS AG | Bahnhofstrasse 18, Spaichingen Baden-Wurttemberg 78549 DE | 2026 | |
| 3043542875 | 3043542875 | MORPHEUS CO., LTD. | Room 1602, 1603, 1604, 120 Heungdeokjungang-ro, Giheung-gu, Yongin-si, Gyeonggi-do, Yongin Gyeonggi 16950 KR | 2026 |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain