Ultroid Technologies, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 4
- 510(k) Clearances
- 0
- Inspections
- 4
- Compliance Actions
- 1
Recent Recalls
| Number | Class | Product | Date |
|---|
| Z-0784-2017 | Class II | Ultroid Procedure Pack including the Ultroid Sterile Disposable Probes. | October 19, 2016 |
| Z-0783-2017 | Class II | Ultroid Mobile Generator/Battery operated unit including the Ultroid Sterile Disposable Probes | October 19, 2016 |
| Z-0782-2017 | Class II | Ultroid Hemorrhoid Management Systems 110/220 VAC and procedures kit including the Ultroid Disposabl | October 19, 2016 |
| Z-0785-2017 | Class II | Ultroid Sterile Disposable Probes sold individually | October 19, 2016 |