International Medical Devices, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 2
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K223051 | Pre-Formed Silicone Block | February 3, 2023 |
| K220760 | Pre-Formed Penile Silicone Block | May 13, 2022 |
| K181387 | Pre-Formed Penile Silicone Block | January 23, 2019 |
| K162624 | Pre-Formed Penile Silicone Block | February 1, 2017 |