Aktormed GmbH
Aktormed GmbH appears in FDA public data with 0 recalls, 5 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on July 20, 2026.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 1
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K261573 | ENDOSCOPE HOLDER (182214) | July 20, 2026 |
| K233312 | SOLOASSIST IID / DEXTER ENDOSCOPE ARM (212499); ARTip solo (202426) + ARTip solo voice (202445); SOL | August 8, 2024 |
| K232405 | ENDOFIX EXO | April 25, 2024 |
| K200473 | SoloAsisst II, Voice Control | December 22, 2020 |
| K171947 | SOLOASSIST II | September 21, 2018 |